Canonical Allele Identifier: CA381934639

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76919826A>T (hg19) ; chr11:g.77208781A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000409709.9:c.6029A>T MANE Select	ENSP00000386331.3:p.Asp2010Val
ENST00000670577.1:c.3830A>T
ENST00000409619.6:c.5882A>T	ENSP00000386635.2:p.Asp1961Val
ENST00000409709.7:c.6029A>T	ENSP00000386331.3:p.Asp2010Val
ENST00000458169.2:c.3455A>T	ENSP00000417017.2:p.Asp1152Val
ENST00000458637.6:c.5915A>T	ENSP00000392185.2:p.Asp1972Val
ENST00000481328.7:n.3565A>T
ENST00000605744.1:n.943A>T
NM_000260.3:c.6029A>T	NP_000251.3:p.Asp2010Val
NM_001127180.1:c.5915A>T	NP_001120652.1:p.Asp1972Val
XM_005274012.2:c.5912A>T	XP_005274069.1:p.Asp1971Val
XM_006718558.2:c.6020A>T	XP_006718621.1:p.Asp2007Val
XM_006718559.2:c.5915A>T	XP_006718622.1:p.Asp1972Val
XM_006718560.2:c.5912A>T	XP_006718623.1:p.Asp1971Val
XM_006718561.2:c.5915A>T	XP_006718624.1:p.Asp1972Val
XM_011545044.1:c.6029A>T	XP_011543346.1:p.Asp2010Val
XM_011545045.1:c.6023A>T	XP_011543347.1:p.Asp2008Val
XM_011545046.1:c.5996A>T	XP_011543348.1:p.Asp1999Val
XM_011545047.1:c.5933A>T	XP_011543349.1:p.Asp1978Val
XM_011545048.1:c.5804A>T	XP_011543350.1:p.Asp1935Val
XM_011545049.1:c.5792A>T	XP_011543351.1:p.Asp1931Val
XM_011545050.1:c.5765A>T	XP_011543352.1:p.Asp1922Val
XM_011545051.1:c.6029A>T	XP_011543353.1:p.Asp2010Val
XR_949938.1:n.6349A>T
XR_949941.1:n.6323A>T
XM_011545044.2:c.6029A>T	XP_011543346.1:p.Asp2010Val
XM_011545046.2:c.6119A>T	XP_011543348.2:p.Asp2040Val
XM_011545050.2:c.5765A>T	XP_011543352.1:p.Asp1922Val
XM_017017778.1:c.6113A>T	XP_016873267.1:p.Asp2038Val
XM_017017779.1:c.6110A>T	XP_016873268.1:p.Asp2037Val
XM_017017780.1:c.6119A>T	XP_016873269.1:p.Asp2040Val
XM_017017781.1:c.6023A>T	XP_016873270.1:p.Asp2008Val
XM_017017782.1:c.6005A>T	XP_016873271.1:p.Asp2002Val
XM_017017783.1:c.6002A>T	XP_016873272.1:p.Asp2001Val
XM_017017784.1:c.6002A>T	XP_016873273.1:p.Asp2001Val
XM_017017785.1:c.5882A>T	XP_016873274.1:p.Asp1961Val
XM_017017786.1:c.6119A>T	XP_016873275.1:p.Asp2040Val
XM_017017788.1:c.6005A>T	XP_016873277.1:p.Asp2002Val
XR_001747885.1:n.6108A>T
XR_001747886.1:n.6049A>T
XR_001747887.1:n.6094A>T
NM_000260.4:c.6029A>T MANE Select	NP_000251.3:p.Asp2010Val
NM_001127180.2:c.5915A>T	NP_001120652.1:p.Asp1972Val
NM_001369365.1:c.5882A>T	NP_001356294.1:p.Asp1961Val