Canonical Allele Identifier: CA1984129919
Gene: MYO7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77211336G= , CM000673.2:g.77211336G= GRCh38
NC_000011.9:g.76922381G= , CM000673.1:g.76922381G= GRCh37
NC_000011.8:g.76600029G= NCBI36
NG_009086.1:g.88072G=
NG_009086.2:g.88091G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.6236G= MANE Select ENSP00000386331.3:p.Arg2079=
ENST00000670577.1:c.4037G=
ENST00000409619.6:c.6089G= ENSP00000386635.2:p.Arg2030=
ENST00000409709.7:c.6236G= ENSP00000386331.3:p.Arg2079=
ENST00000458169.2:c.3662G= ENSP00000417017.2:p.Arg1221=
ENST00000458637.6:c.6122G= ENSP00000392185.2:p.Arg2041=
ENST00000481328.7:n.3772G=
ENST00000526863.2:n.25+425G=
ENST00000605744.1:n.1703G=
NM_000260.3:c.6236G= NP_000251.3:p.Arg2079=
NM_001127180.1:c.6122G= NP_001120652.1:p.Arg2041=
XM_005274012.2:c.6119G= XP_005274069.1:p.Arg2040=
XM_006718558.2:c.6227G= XP_006718621.1:p.Arg2076=
XM_006718559.2:c.6122G= XP_006718622.1:p.Arg2041=
XM_006718560.2:c.6119G= XP_006718623.1:p.Arg2040=
XM_006718561.2:c.6122G= XP_006718624.1:p.Arg2041=
XM_011545044.1:c.6236G= XP_011543346.1:p.Arg2079=
XM_011545045.1:c.6230G= XP_011543347.1:p.Arg2077=
XM_011545046.1:c.6203G= XP_011543348.1:p.Arg2068=
XM_011545047.1:c.6140G= XP_011543349.1:p.Arg2047=
XM_011545048.1:c.6011G= XP_011543350.1:p.Arg2004=
XM_011545049.1:c.5999G= XP_011543351.1:p.Arg2000=
XM_011545050.1:c.5972G= XP_011543352.1:p.Arg1991=
XM_011545051.1:c.6236G= XP_011543353.1:p.Arg2079=
XR_949938.1:n.6556G=
XR_949941.1:n.6530G=
XM_011545044.2:c.6236G= XP_011543346.1:p.Arg2079=
XM_011545046.2:c.6326G= XP_011543348.2:p.Arg2109=
XM_011545050.2:c.5972G= XP_011543352.1:p.Arg1991=
XM_017017778.1:c.6320G= XP_016873267.1:p.Arg2107=
XM_017017779.1:c.6317G= XP_016873268.1:p.Arg2106=
XM_017017780.1:c.6326G= XP_016873269.1:p.Arg2109=
XM_017017781.1:c.6230G= XP_016873270.1:p.Arg2077=
XM_017017782.1:c.6212G= XP_016873271.1:p.Arg2071=
XM_017017783.1:c.6209G= XP_016873272.1:p.Arg2070=
XM_017017784.1:c.6209G= XP_016873273.1:p.Arg2070=
XM_017017785.1:c.6089G= XP_016873274.1:p.Arg2030=
XM_017017786.1:c.6326G= XP_016873275.1:p.Arg2109=
XM_017017788.1:c.6212G= XP_016873277.1:p.Arg2071=
XR_001747885.1:n.6315G=
XR_001747887.1:n.6301G=
NM_000260.4:c.6236G= MANE Select NP_000251.3:p.Arg2079=
NM_001127180.2:c.6122G= NP_001120652.1:p.Arg2041=
NM_001369365.1:c.6089G= NP_001356294.1:p.Arg2030=