Canonical Allele Identifier: CA381946914
Gene: MYO7A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77189386C>G , CM000673.2:g.77189386C>G GRCh38
NC_000011.9:g.76900431C>G , CM000673.1:g.76900431C>G GRCh37
NC_000011.8:g.76578079C>G NCBI36
NG_009086.1:g.66122C>G
NG_009086.2:g.66141C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.3546C>G MANE Select ENSP00000386331.3:p.Asn1182Lys
ENST00000670577.1:c.1387C>G
ENST00000409619.6:c.3513C>G ENSP00000386635.2:p.Asn1171Lys
ENST00000409709.7:c.3546C>G ENSP00000386331.3:p.Asn1182Lys
ENST00000458169.2:c.1089C>G ENSP00000417017.2:p.Asn363Lys
ENST00000458637.6:c.3546C>G ENSP00000392185.2:p.Asn1182Lys
ENST00000467137.1:n.73C>G
ENST00000481328.7:n.1089C>G
NM_000260.3:c.3546C>G NP_000251.3:p.Asn1182Lys
NM_001127180.1:c.3546C>G NP_001120652.1:p.Asn1182Lys
XM_005274012.2:c.3546C>G XP_005274069.1:p.Asn1182Lys
XM_006718558.2:c.3546C>G XP_006718621.1:p.Asn1182Lys
XM_006718559.2:c.3546C>G XP_006718622.1:p.Asn1182Lys
XM_006718560.2:c.3546C>G XP_006718623.1:p.Asn1182Lys
XM_006718561.2:c.3546C>G XP_006718624.1:p.Asn1182Lys
XM_011545044.1:c.3546C>G XP_011543346.1:p.Asn1182Lys
XM_011545045.1:c.3546C>G XP_011543347.1:p.Asn1182Lys
XM_011545046.1:c.3513C>G XP_011543348.1:p.Asn1171Lys
XM_011545047.1:c.3456C>G XP_011543349.1:p.Asn1152Lys
XM_011545048.1:c.3327C>G XP_011543350.1:p.Asn1109Lys
XM_011545049.1:c.3315C>G XP_011543351.1:p.Asn1105Lys
XM_011545050.1:c.3288C>G XP_011543352.1:p.Asn1096Lys
XM_011545051.1:c.3546C>G XP_011543353.1:p.Asn1182Lys
XM_011545052.1:c.3546C>G XP_011543354.1:p.Asn1182Lys
XR_949938.1:n.3866C>G
XR_949941.1:n.3866C>G
XR_949942.1:n.3868C>G
XR_949943.1:n.3868C>G
XM_011545044.2:c.3546C>G XP_011543346.1:p.Asn1182Lys
XM_011545046.2:c.3636C>G XP_011543348.2:p.Asn1212Lys
XM_011545050.2:c.3288C>G XP_011543352.1:p.Asn1096Lys
XM_017017778.1:c.3636C>G XP_016873267.1:p.Asn1212Lys
XM_017017779.1:c.3636C>G XP_016873268.1:p.Asn1212Lys
XM_017017780.1:c.3636C>G XP_016873269.1:p.Asn1212Lys
XM_017017781.1:c.3546C>G XP_016873270.1:p.Asn1182Lys
XM_017017782.1:c.3636C>G XP_016873271.1:p.Asn1212Lys
XM_017017783.1:c.3636C>G XP_016873272.1:p.Asn1212Lys
XM_017017784.1:c.3636C>G XP_016873273.1:p.Asn1212Lys
XM_017017785.1:c.3405C>G XP_016873274.1:p.Asn1135Lys
XM_017017786.1:c.3636C>G XP_016873275.1:p.Asn1212Lys
XM_017017787.1:c.3636C>G XP_016873276.1:p.Asn1212Lys
XM_017017788.1:c.3636C>G XP_016873277.1:p.Asn1212Lys
XR_001747885.1:n.3651C>G
XR_001747886.1:n.3651C>G
XR_001747887.1:n.3651C>G
XR_001747888.1:n.3651C>G
XR_001747889.1:n.3651C>G
NM_000260.4:c.3546C>G MANE Select NP_000251.3:p.Asn1182Lys
NM_001127180.2:c.3546C>G NP_001120652.1:p.Asn1182Lys
NM_001369365.1:c.3513C>G NP_001356294.1:p.Asn1171Lys