Canonical Allele Identifier: CA2792769062
Gene: MYO7A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77172953_77172954insGAC , CM000673.2:g.77172953_77172954insGAC GRCh38
NC_000011.9:g.76883999_76884000insGAC , CM000673.1:g.76883999_76884000insGAC GRCh37
NC_000011.8:g.76561647_76561648insGAC NCBI36
NG_009086.1:g.49690_49691insGAC
NG_009086.2:g.49708_49709insGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.1935+68_1935+69insGAC MANE Select ENSP00000386331.3:n.1935+68_1935+69insGAC
ENST00000409619.6:c.1902+68_1902+69insGAC ENSP00000386635.2:n.1902+68_1902+69insGAC
ENST00000409709.7:c.1935+68_1935+69insGAC ENSP00000386331.3:n.1935+68_1935+69insGAC
ENST00000409893.5:c.1935+68_1935+69insGAC ENSP00000386689.1:n.1935+68_1935+69insGAC
ENST00000458637.6:c.1935+68_1935+69insGAC ENSP00000392185.2:n.1935+68_1935+69insGAC
ENST00000620575.4:c.1935+68_1935+69insGAC ENSP00000477640.1:n.1935+68_1935+69insGAC
NM_000260.3:c.1935+68_1935+69insGAC NP_000251.3:n.1935+68_1935+69insGAC
NM_001127179.2:c.1935+68_1935+69insGAC NP_001120651.2:n.1935+68_1935+69insGAC
NM_001127180.1:c.1935+68_1935+69insGAC NP_001120652.1:n.1935+68_1935+69insGAC
XM_005274012.2:c.1935+68_1935+69insGAC XP_005274069.1:n.1935+68_1935+69insGAC
XM_006718558.2:c.1935+68_1935+69insGAC XP_006718621.1:n.1935+68_1935+69insGAC
XM_006718559.2:c.1935+68_1935+69insGAC XP_006718622.1:n.1935+68_1935+69insGAC
XM_006718560.2:c.1935+68_1935+69insGAC XP_006718623.1:n.1935+68_1935+69insGAC
XM_006718561.2:c.1935+68_1935+69insGAC XP_006718624.1:n.1935+68_1935+69insGAC
XM_011545044.1:c.1935+68_1935+69insGAC XP_011543346.1:n.1935+68_1935+69insGAC
XM_011545045.1:c.1935+68_1935+69insGAC XP_011543347.1:n.1935+68_1935+69insGAC
XM_011545046.1:c.1902+68_1902+69insGAC XP_011543348.1:n.1902+68_1902+69insGAC
XM_011545047.1:c.1935+68_1935+69insGAC XP_011543349.1:n.1935+68_1935+69insGAC
XM_011545048.1:c.1935+68_1935+69insGAC XP_011543350.1:n.1935+68_1935+69insGAC
XM_011545049.1:c.1704+68_1704+69insGAC XP_011543351.1:n.1704+68_1704+69insGAC
XM_011545050.1:c.1677+68_1677+69insGAC XP_011543352.1:n.1677+68_1677+69insGAC
XM_011545051.1:c.1935+68_1935+69insGAC XP_011543353.1:n.1935+68_1935+69insGAC
XM_011545052.1:c.1935+68_1935+69insGAC XP_011543354.1:n.1935+68_1935+69insGAC
XR_949938.1:n.2255+68_2255+69insGAC
XR_949941.1:n.2255+68_2255+69insGAC
XR_949942.1:n.2257+68_2257+69insGAC
XR_949943.1:n.2257+68_2257+69insGAC
XM_011545044.2:c.1935+68_1935+69insGAC XP_011543346.1:n.1935+68_1935+69insGAC
XM_011545046.2:c.2025+68_2025+69insGAC XP_011543348.2:n.2025+68_2025+69insGAC
XM_011545050.2:c.1677+68_1677+69insGAC XP_011543352.1:n.1677+68_1677+69insGAC
XM_017017778.1:c.2025+68_2025+69insGAC XP_016873267.1:n.2025+68_2025+69insGAC
XM_017017779.1:c.2025+68_2025+69insGAC XP_016873268.1:n.2025+68_2025+69insGAC
XM_017017780.1:c.2025+68_2025+69insGAC XP_016873269.1:n.2025+68_2025+69insGAC
XM_017017781.1:c.2025+68_2025+69insGAC XP_016873270.1:n.2025+68_2025+69insGAC
XM_017017782.1:c.2025+68_2025+69insGAC XP_016873271.1:n.2025+68_2025+69insGAC
XM_017017783.1:c.2025+68_2025+69insGAC XP_016873272.1:n.2025+68_2025+69insGAC
XM_017017784.1:c.2025+68_2025+69insGAC XP_016873273.1:n.2025+68_2025+69insGAC
XM_017017785.1:c.1794+68_1794+69insGAC XP_016873274.1:n.1794+68_1794+69insGAC
XM_017017786.1:c.2025+68_2025+69insGAC XP_016873275.1:n.2025+68_2025+69insGAC
XM_017017787.1:c.2025+68_2025+69insGAC XP_016873276.1:n.2025+68_2025+69insGAC
XM_017017788.1:c.2025+68_2025+69insGAC XP_016873277.1:n.2025+68_2025+69insGAC
XR_001747885.1:n.2040+68_2040+69insGAC
XR_001747886.1:n.2040+68_2040+69insGAC
XR_001747887.1:n.2040+68_2040+69insGAC
XR_001747888.1:n.2040+68_2040+69insGAC
XR_001747889.1:n.2040+68_2040+69insGAC
NM_000260.4:c.1935+68_1935+69insGAC MANE Select NP_000251.3:n.1935+68_1935+69insGAC
NM_001127180.2:c.1935+68_1935+69insGAC NP_001120652.1:n.1935+68_1935+69insGAC
NM_001369365.1:c.1902+68_1902+69insGAC NP_001356294.1:n.1902+68_1902+69insGAC
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