Canonical Allele Identifier: CA2792769064
Gene: MYO7A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77172960_77172961insACAC , CM000673.2:g.77172960_77172961insACAC GRCh38
NC_000011.9:g.76884006_76884007insACAC , CM000673.1:g.76884006_76884007insACAC GRCh37
NC_000011.8:g.76561654_76561655insACAC NCBI36
NG_009086.1:g.49697_49698insACAC
NG_009086.2:g.49715_49716insACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.1935+75_1935+76insACAC MANE Select ENSP00000386331.3:n.1935+75_1935+76insACAC
ENST00000409619.6:c.1902+75_1902+76insACAC ENSP00000386635.2:n.1902+75_1902+76insACAC
ENST00000409709.7:c.1935+75_1935+76insACAC ENSP00000386331.3:n.1935+75_1935+76insACAC
ENST00000409893.5:c.1935+75_1935+76insACAC ENSP00000386689.1:n.1935+75_1935+76insACAC
ENST00000458637.6:c.1935+75_1935+76insACAC ENSP00000392185.2:n.1935+75_1935+76insACAC
ENST00000620575.4:c.1935+75_1935+76insACAC ENSP00000477640.1:n.1935+75_1935+76insACAC
NM_000260.3:c.1935+75_1935+76insACAC NP_000251.3:n.1935+75_1935+76insACAC
NM_001127179.2:c.1935+75_1935+76insACAC NP_001120651.2:n.1935+75_1935+76insACAC
NM_001127180.1:c.1935+75_1935+76insACAC NP_001120652.1:n.1935+75_1935+76insACAC
XM_005274012.2:c.1935+75_1935+76insACAC XP_005274069.1:n.1935+75_1935+76insACAC
XM_006718558.2:c.1935+75_1935+76insACAC XP_006718621.1:n.1935+75_1935+76insACAC
XM_006718559.2:c.1935+75_1935+76insACAC XP_006718622.1:n.1935+75_1935+76insACAC
XM_006718560.2:c.1935+75_1935+76insACAC XP_006718623.1:n.1935+75_1935+76insACAC
XM_006718561.2:c.1935+75_1935+76insACAC XP_006718624.1:n.1935+75_1935+76insACAC
XM_011545044.1:c.1935+75_1935+76insACAC XP_011543346.1:n.1935+75_1935+76insACAC
XM_011545045.1:c.1935+75_1935+76insACAC XP_011543347.1:n.1935+75_1935+76insACAC
XM_011545046.1:c.1902+75_1902+76insACAC XP_011543348.1:n.1902+75_1902+76insACAC
XM_011545047.1:c.1935+75_1935+76insACAC XP_011543349.1:n.1935+75_1935+76insACAC
XM_011545048.1:c.1935+75_1935+76insACAC XP_011543350.1:n.1935+75_1935+76insACAC
XM_011545049.1:c.1704+75_1704+76insACAC XP_011543351.1:n.1704+75_1704+76insACAC
XM_011545050.1:c.1677+75_1677+76insACAC XP_011543352.1:n.1677+75_1677+76insACAC
XM_011545051.1:c.1935+75_1935+76insACAC XP_011543353.1:n.1935+75_1935+76insACAC
XM_011545052.1:c.1935+75_1935+76insACAC XP_011543354.1:n.1935+75_1935+76insACAC
XR_949938.1:n.2255+75_2255+76insACAC
XR_949941.1:n.2255+75_2255+76insACAC
XR_949942.1:n.2257+75_2257+76insACAC
XR_949943.1:n.2257+75_2257+76insACAC
XM_011545044.2:c.1935+75_1935+76insACAC XP_011543346.1:n.1935+75_1935+76insACAC
XM_011545046.2:c.2025+75_2025+76insACAC XP_011543348.2:n.2025+75_2025+76insACAC
XM_011545050.2:c.1677+75_1677+76insACAC XP_011543352.1:n.1677+75_1677+76insACAC
XM_017017778.1:c.2025+75_2025+76insACAC XP_016873267.1:n.2025+75_2025+76insACAC
XM_017017779.1:c.2025+75_2025+76insACAC XP_016873268.1:n.2025+75_2025+76insACAC
XM_017017780.1:c.2025+75_2025+76insACAC XP_016873269.1:n.2025+75_2025+76insACAC
XM_017017781.1:c.2025+75_2025+76insACAC XP_016873270.1:n.2025+75_2025+76insACAC
XM_017017782.1:c.2025+75_2025+76insACAC XP_016873271.1:n.2025+75_2025+76insACAC
XM_017017783.1:c.2025+75_2025+76insACAC XP_016873272.1:n.2025+75_2025+76insACAC
XM_017017784.1:c.2025+75_2025+76insACAC XP_016873273.1:n.2025+75_2025+76insACAC
XM_017017785.1:c.1794+75_1794+76insACAC XP_016873274.1:n.1794+75_1794+76insACAC
XM_017017786.1:c.2025+75_2025+76insACAC XP_016873275.1:n.2025+75_2025+76insACAC
XM_017017787.1:c.2025+75_2025+76insACAC XP_016873276.1:n.2025+75_2025+76insACAC
XM_017017788.1:c.2025+75_2025+76insACAC XP_016873277.1:n.2025+75_2025+76insACAC
XR_001747885.1:n.2040+75_2040+76insACAC
XR_001747886.1:n.2040+75_2040+76insACAC
XR_001747887.1:n.2040+75_2040+76insACAC
XR_001747888.1:n.2040+75_2040+76insACAC
XR_001747889.1:n.2040+75_2040+76insACAC
NM_000260.4:c.1935+75_1935+76insACAC MANE Select NP_000251.3:n.1935+75_1935+76insACAC
NM_001127180.2:c.1935+75_1935+76insACAC NP_001120652.1:n.1935+75_1935+76insACAC
NM_001369365.1:c.1902+75_1902+76insACAC NP_001356294.1:n.1902+75_1902+76insACAC
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