Canonical Allele Identifier: CA381936259

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76922360T>A (hg19) ; chr11:g.77211315T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211315T>A , CM000673.2:g.77211315T>A	GRCh38
NC_000011.9:g.76922360T>A , CM000673.1:g.76922360T>A	GRCh37
NC_000011.8:g.76600008T>A	NCBI36
NG_009086.1:g.88051T>A
NG_009086.2:g.88070T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000409709.9:c.6215T>A MANE Select	ENSP00000386331.3:p.Val2072Asp
ENST00000670577.1:c.4016T>A
ENST00000409619.6:c.6068T>A	ENSP00000386635.2:p.Val2023Asp
ENST00000409709.7:c.6215T>A	ENSP00000386331.3:p.Val2072Asp
ENST00000458169.2:c.3641T>A	ENSP00000417017.2:p.Val1214Asp
ENST00000458637.6:c.6101T>A	ENSP00000392185.2:p.Val2034Asp
ENST00000481328.7:n.3751T>A
ENST00000526863.2:n.25+404T>A
ENST00000605744.1:n.1682T>A
NM_000260.3:c.6215T>A	NP_000251.3:p.Val2072Asp
NM_001127180.1:c.6101T>A	NP_001120652.1:p.Val2034Asp
XM_005274012.2:c.6098T>A	XP_005274069.1:p.Val2033Asp
XM_006718558.2:c.6206T>A	XP_006718621.1:p.Val2069Asp
XM_006718559.2:c.6101T>A	XP_006718622.1:p.Val2034Asp
XM_006718560.2:c.6098T>A	XP_006718623.1:p.Val2033Asp
XM_006718561.2:c.6101T>A	XP_006718624.1:p.Val2034Asp
XM_011545044.1:c.6215T>A	XP_011543346.1:p.Val2072Asp
XM_011545045.1:c.6209T>A	XP_011543347.1:p.Val2070Asp
XM_011545046.1:c.6182T>A	XP_011543348.1:p.Val2061Asp
XM_011545047.1:c.6119T>A	XP_011543349.1:p.Val2040Asp
XM_011545048.1:c.5990T>A	XP_011543350.1:p.Val1997Asp
XM_011545049.1:c.5978T>A	XP_011543351.1:p.Val1993Asp
XM_011545050.1:c.5951T>A	XP_011543352.1:p.Val1984Asp
XM_011545051.1:c.6215T>A	XP_011543353.1:p.Val2072Asp
XR_949938.1:n.6535T>A
XR_949941.1:n.6509T>A
XM_011545044.2:c.6215T>A	XP_011543346.1:p.Val2072Asp
XM_011545046.2:c.6305T>A	XP_011543348.2:p.Val2102Asp
XM_011545050.2:c.5951T>A	XP_011543352.1:p.Val1984Asp
XM_017017778.1:c.6299T>A	XP_016873267.1:p.Val2100Asp
XM_017017779.1:c.6296T>A	XP_016873268.1:p.Val2099Asp
XM_017017780.1:c.6305T>A	XP_016873269.1:p.Val2102Asp
XM_017017781.1:c.6209T>A	XP_016873270.1:p.Val2070Asp
XM_017017782.1:c.6191T>A	XP_016873271.1:p.Val2064Asp
XM_017017783.1:c.6188T>A	XP_016873272.1:p.Val2063Asp
XM_017017784.1:c.6188T>A	XP_016873273.1:p.Val2063Asp
XM_017017785.1:c.6068T>A	XP_016873274.1:p.Val2023Asp
XM_017017786.1:c.6305T>A	XP_016873275.1:p.Val2102Asp
XM_017017788.1:c.6191T>A	XP_016873277.1:p.Val2064Asp
XR_001747885.1:n.6294T>A
XR_001747887.1:n.6280T>A
NM_000260.4:c.6215T>A MANE Select	NP_000251.3:p.Val2072Asp
NM_001127180.2:c.6101T>A	NP_001120652.1:p.Val2034Asp
NM_001369365.1:c.6068T>A	NP_001356294.1:p.Val2023Asp