Canonical Allele Identifier: CA1984128611
Gene: MYO7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77208781A= , CM000673.2:g.77208781A= GRCh38
NC_000011.9:g.76919826A= , CM000673.1:g.76919826A= GRCh37
NC_000011.8:g.76597474A= NCBI36
NG_009086.1:g.85517A=
NG_009086.2:g.85536A=

Transcript Alleles

HGVS Amino-acid change
ENST00000409709.9:c.6029A= MANE Select ENSP00000386331.3:p.Asp2010=
ENST00000670577.1:c.3830A=
ENST00000409619.6:c.5882A= ENSP00000386635.2:p.Asp1961=
ENST00000409709.7:c.6029A= ENSP00000386331.3:p.Asp2010=
ENST00000458169.2:c.3455A= ENSP00000417017.2:p.Asp1152=
ENST00000458637.6:c.5915A= ENSP00000392185.2:p.Asp1972=
ENST00000481328.7:n.3565A=
ENST00000605744.1:n.943A=
NM_000260.3:c.6029A= NP_000251.3:p.Asp2010=
NM_001127180.1:c.5915A= NP_001120652.1:p.Asp1972=
XM_005274012.2:c.5912A= XP_005274069.1:p.Asp1971=
XM_006718558.2:c.6020A= XP_006718621.1:p.Asp2007=
XM_006718559.2:c.5915A= XP_006718622.1:p.Asp1972=
XM_006718560.2:c.5912A= XP_006718623.1:p.Asp1971=
XM_006718561.2:c.5915A= XP_006718624.1:p.Asp1972=
XM_011545044.1:c.6029A= XP_011543346.1:p.Asp2010=
XM_011545045.1:c.6023A= XP_011543347.1:p.Asp2008=
XM_011545046.1:c.5996A= XP_011543348.1:p.Asp1999=
XM_011545047.1:c.5933A= XP_011543349.1:p.Asp1978=
XM_011545048.1:c.5804A= XP_011543350.1:p.Asp1935=
XM_011545049.1:c.5792A= XP_011543351.1:p.Asp1931=
XM_011545050.1:c.5765A= XP_011543352.1:p.Asp1922=
XM_011545051.1:c.6029A= XP_011543353.1:p.Asp2010=
XR_949938.1:n.6349A=
XR_949941.1:n.6323A=
XM_011545044.2:c.6029A= XP_011543346.1:p.Asp2010=
XM_011545046.2:c.6119A= XP_011543348.2:p.Asp2040=
XM_011545050.2:c.5765A= XP_011543352.1:p.Asp1922=
XM_017017778.1:c.6113A= XP_016873267.1:p.Asp2038=
XM_017017779.1:c.6110A= XP_016873268.1:p.Asp2037=
XM_017017780.1:c.6119A= XP_016873269.1:p.Asp2040=
XM_017017781.1:c.6023A= XP_016873270.1:p.Asp2008=
XM_017017782.1:c.6005A= XP_016873271.1:p.Asp2002=
XM_017017783.1:c.6002A= XP_016873272.1:p.Asp2001=
XM_017017784.1:c.6002A= XP_016873273.1:p.Asp2001=
XM_017017785.1:c.5882A= XP_016873274.1:p.Asp1961=
XM_017017786.1:c.6119A= XP_016873275.1:p.Asp2040=
XM_017017788.1:c.6005A= XP_016873277.1:p.Asp2002=
XR_001747885.1:n.6108A=
XR_001747886.1:n.6049A=
XR_001747887.1:n.6094A=
NM_000260.4:c.6029A= MANE Select NP_000251.3:p.Asp2010=
NM_001127180.2:c.5915A= NP_001120652.1:p.Asp1972=
NM_001369365.1:c.5882A= NP_001356294.1:p.Asp1961=