Canonical Allele Identifier: CA1984123119
Gene: MYO7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77190069G= , CM000673.2:g.77190069G= GRCh38
NC_000011.9:g.76901114G= , CM000673.1:g.76901114G= GRCh37
NC_000011.8:g.76578762G= NCBI36
NG_009086.1:g.66805G=
NG_009086.2:g.66824G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.3680G= MANE Select ENSP00000386331.3:p.Cys1227=
ENST00000670577.1:c.1521G=
ENST00000409619.6:c.3647G= ENSP00000386635.2:p.Cys1216=
ENST00000409709.7:c.3680G= ENSP00000386331.3:p.Cys1227=
ENST00000458169.2:c.1223G= ENSP00000417017.2:p.Cys408=
ENST00000458637.6:c.3680G= ENSP00000392185.2:p.Cys1227=
ENST00000467137.1:n.207G=
ENST00000481328.7:n.1223G=
NM_000260.3:c.3680G= NP_000251.3:p.Cys1227=
NM_001127180.1:c.3680G= NP_001120652.1:p.Cys1227=
XM_005274012.2:c.3680G= XP_005274069.1:p.Cys1227=
XM_006718558.2:c.3680G= XP_006718621.1:p.Cys1227=
XM_006718559.2:c.3680G= XP_006718622.1:p.Cys1227=
XM_006718560.2:c.3680G= XP_006718623.1:p.Cys1227=
XM_006718561.2:c.3680G= XP_006718624.1:p.Cys1227=
XM_011545044.1:c.3680G= XP_011543346.1:p.Cys1227=
XM_011545045.1:c.3680G= XP_011543347.1:p.Cys1227=
XM_011545046.1:c.3647G= XP_011543348.1:p.Cys1216=
XM_011545047.1:c.3590G= XP_011543349.1:p.Cys1197=
XM_011545048.1:c.3461G= XP_011543350.1:p.Cys1154=
XM_011545049.1:c.3449G= XP_011543351.1:p.Cys1150=
XM_011545050.1:c.3422G= XP_011543352.1:p.Cys1141=
XM_011545051.1:c.3680G= XP_011543353.1:p.Cys1227=
XM_011545052.1:c.3680G= XP_011543354.1:p.Cys1227=
XR_949938.1:n.4000G=
XR_949941.1:n.4000G=
XR_949942.1:n.4002G=
XR_949943.1:n.4002G=
XM_011545044.2:c.3680G= XP_011543346.1:p.Cys1227=
XM_011545046.2:c.3770G= XP_011543348.2:p.Cys1257=
XM_011545050.2:c.3422G= XP_011543352.1:p.Cys1141=
XM_017017778.1:c.3770G= XP_016873267.1:p.Cys1257=
XM_017017779.1:c.3770G= XP_016873268.1:p.Cys1257=
XM_017017780.1:c.3770G= XP_016873269.1:p.Cys1257=
XM_017017781.1:c.3680G= XP_016873270.1:p.Cys1227=
XM_017017782.1:c.3770G= XP_016873271.1:p.Cys1257=
XM_017017783.1:c.3770G= XP_016873272.1:p.Cys1257=
XM_017017784.1:c.3770G= XP_016873273.1:p.Cys1257=
XM_017017785.1:c.3539G= XP_016873274.1:p.Cys1180=
XM_017017786.1:c.3770G= XP_016873275.1:p.Cys1257=
XM_017017787.1:c.3770G= XP_016873276.1:p.Cys1257=
XM_017017788.1:c.3770G= XP_016873277.1:p.Cys1257=
XR_001747885.1:n.3785G=
XR_001747886.1:n.3785G=
XR_001747887.1:n.3785G=
XR_001747888.1:n.3785G=
XR_001747889.1:n.3785G=
NM_000260.4:c.3680G= MANE Select NP_000251.3:p.Cys1227=
NM_001127180.2:c.3680G= NP_001120652.1:p.Cys1227=
NM_001369365.1:c.3647G= NP_001356294.1:p.Cys1216=