Canonical Allele Identifier: CA1984128614
Gene: MYO7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77208788C= , CM000673.2:g.77208788C= GRCh38
NC_000011.9:g.76919833C= , CM000673.1:g.76919833C= GRCh37
NC_000011.8:g.76597481C= NCBI36
NG_009086.1:g.85524C=
NG_009086.2:g.85543C=

Transcript Alleles

HGVS Amino-acid change
ENST00000409709.9:c.6036C= MANE Select ENSP00000386331.3:p.Ile2012=
ENST00000670577.1:c.3837C=
ENST00000409619.6:c.5889C= ENSP00000386635.2:p.Ile1963=
ENST00000409709.7:c.6036C= ENSP00000386331.3:p.Ile2012=
ENST00000458169.2:c.3462C= ENSP00000417017.2:p.Ile1154=
ENST00000458637.6:c.5922C= ENSP00000392185.2:p.Ile1974=
ENST00000481328.7:n.3572C=
ENST00000605744.1:n.950C=
NM_000260.3:c.6036C= NP_000251.3:p.Ile2012=
NM_001127180.1:c.5922C= NP_001120652.1:p.Ile1974=
XM_005274012.2:c.5919C= XP_005274069.1:p.Ile1973=
XM_006718558.2:c.6027C= XP_006718621.1:p.Ile2009=
XM_006718559.2:c.5922C= XP_006718622.1:p.Ile1974=
XM_006718560.2:c.5919C= XP_006718623.1:p.Ile1973=
XM_006718561.2:c.5922C= XP_006718624.1:p.Ile1974=
XM_011545044.1:c.6036C= XP_011543346.1:p.Ile2012=
XM_011545045.1:c.6030C= XP_011543347.1:p.Ile2010=
XM_011545046.1:c.6003C= XP_011543348.1:p.Ile2001=
XM_011545047.1:c.5940C= XP_011543349.1:p.Ile1980=
XM_011545048.1:c.5811C= XP_011543350.1:p.Ile1937=
XM_011545049.1:c.5799C= XP_011543351.1:p.Ile1933=
XM_011545050.1:c.5772C= XP_011543352.1:p.Ile1924=
XM_011545051.1:c.6036C= XP_011543353.1:p.Ile2012=
XR_949938.1:n.6356C=
XR_949941.1:n.6330C=
XM_011545044.2:c.6036C= XP_011543346.1:p.Ile2012=
XM_011545046.2:c.6126C= XP_011543348.2:p.Ile2042=
XM_011545050.2:c.5772C= XP_011543352.1:p.Ile1924=
XM_017017778.1:c.6120C= XP_016873267.1:p.Ile2040=
XM_017017779.1:c.6117C= XP_016873268.1:p.Ile2039=
XM_017017780.1:c.6126C= XP_016873269.1:p.Ile2042=
XM_017017781.1:c.6030C= XP_016873270.1:p.Ile2010=
XM_017017782.1:c.6012C= XP_016873271.1:p.Ile2004=
XM_017017783.1:c.6009C= XP_016873272.1:p.Ile2003=
XM_017017784.1:c.6009C= XP_016873273.1:p.Ile2003=
XM_017017785.1:c.5889C= XP_016873274.1:p.Ile1963=
XM_017017786.1:c.6126C= XP_016873275.1:p.Ile2042=
XM_017017788.1:c.6012C= XP_016873277.1:p.Ile2004=
XR_001747885.1:n.6115C=
XR_001747886.1:n.6056C=
XR_001747887.1:n.6101C=
NM_000260.4:c.6036C= MANE Select NP_000251.3:p.Ile2012=
NM_001127180.2:c.5922C= NP_001120652.1:p.Ile1974=
NM_001369365.1:c.5889C= NP_001356294.1:p.Ile1963=