Canonical Allele Identifier: CA1984128613
Gene: MYO7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77208786A= , CM000673.2:g.77208786A= GRCh38
NC_000011.9:g.76919831A= , CM000673.1:g.76919831A= GRCh37
NC_000011.8:g.76597479A= NCBI36
NG_009086.1:g.85522A=
NG_009086.2:g.85541A=

Transcript Alleles

HGVS Amino-acid change
ENST00000409709.9:c.6034A= MANE Select ENSP00000386331.3:p.Ile2012=
ENST00000670577.1:c.3835A=
ENST00000409619.6:c.5887A= ENSP00000386635.2:p.Ile1963=
ENST00000409709.7:c.6034A= ENSP00000386331.3:p.Ile2012=
ENST00000458169.2:c.3460A= ENSP00000417017.2:p.Ile1154=
ENST00000458637.6:c.5920A= ENSP00000392185.2:p.Ile1974=
ENST00000481328.7:n.3570A=
ENST00000605744.1:n.948A=
NM_000260.3:c.6034A= NP_000251.3:p.Ile2012=
NM_001127180.1:c.5920A= NP_001120652.1:p.Ile1974=
XM_005274012.2:c.5917A= XP_005274069.1:p.Ile1973=
XM_006718558.2:c.6025A= XP_006718621.1:p.Ile2009=
XM_006718559.2:c.5920A= XP_006718622.1:p.Ile1974=
XM_006718560.2:c.5917A= XP_006718623.1:p.Ile1973=
XM_006718561.2:c.5920A= XP_006718624.1:p.Ile1974=
XM_011545044.1:c.6034A= XP_011543346.1:p.Ile2012=
XM_011545045.1:c.6028A= XP_011543347.1:p.Ile2010=
XM_011545046.1:c.6001A= XP_011543348.1:p.Ile2001=
XM_011545047.1:c.5938A= XP_011543349.1:p.Ile1980=
XM_011545048.1:c.5809A= XP_011543350.1:p.Ile1937=
XM_011545049.1:c.5797A= XP_011543351.1:p.Ile1933=
XM_011545050.1:c.5770A= XP_011543352.1:p.Ile1924=
XM_011545051.1:c.6034A= XP_011543353.1:p.Ile2012=
XR_949938.1:n.6354A=
XR_949941.1:n.6328A=
XM_011545044.2:c.6034A= XP_011543346.1:p.Ile2012=
XM_011545046.2:c.6124A= XP_011543348.2:p.Ile2042=
XM_011545050.2:c.5770A= XP_011543352.1:p.Ile1924=
XM_017017778.1:c.6118A= XP_016873267.1:p.Ile2040=
XM_017017779.1:c.6115A= XP_016873268.1:p.Ile2039=
XM_017017780.1:c.6124A= XP_016873269.1:p.Ile2042=
XM_017017781.1:c.6028A= XP_016873270.1:p.Ile2010=
XM_017017782.1:c.6010A= XP_016873271.1:p.Ile2004=
XM_017017783.1:c.6007A= XP_016873272.1:p.Ile2003=
XM_017017784.1:c.6007A= XP_016873273.1:p.Ile2003=
XM_017017785.1:c.5887A= XP_016873274.1:p.Ile1963=
XM_017017786.1:c.6124A= XP_016873275.1:p.Ile2042=
XM_017017788.1:c.6010A= XP_016873277.1:p.Ile2004=
XR_001747885.1:n.6113A=
XR_001747886.1:n.6054A=
XR_001747887.1:n.6099A=
NM_000260.4:c.6034A= MANE Select NP_000251.3:p.Ile2012=
NM_001127180.2:c.5920A= NP_001120652.1:p.Ile1974=
NM_001369365.1:c.5887A= NP_001356294.1:p.Ile1963=