Canonical Allele Identifier: CA381934643

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76919827T>A (hg19) ; chr11:g.77208782T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77208782T>A , CM000673.2:g.77208782T>A	GRCh38
NC_000011.9:g.76919827T>A , CM000673.1:g.76919827T>A	GRCh37
NC_000011.8:g.76597475T>A	NCBI36
NG_009086.1:g.85518T>A
NG_009086.2:g.85537T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000409709.9:c.6030T>A MANE Select	ENSP00000386331.3:p.Asp2010Glu
ENST00000670577.1:c.3831T>A
ENST00000409619.6:c.5883T>A	ENSP00000386635.2:p.Asp1961Glu
ENST00000409709.7:c.6030T>A	ENSP00000386331.3:p.Asp2010Glu
ENST00000458169.2:c.3456T>A	ENSP00000417017.2:p.Asp1152Glu
ENST00000458637.6:c.5916T>A	ENSP00000392185.2:p.Asp1972Glu
ENST00000481328.7:n.3566T>A
ENST00000605744.1:n.944T>A
NM_000260.3:c.6030T>A	NP_000251.3:p.Asp2010Glu
NM_001127180.1:c.5916T>A	NP_001120652.1:p.Asp1972Glu
XM_005274012.2:c.5913T>A	XP_005274069.1:p.Asp1971Glu
XM_006718558.2:c.6021T>A	XP_006718621.1:p.Asp2007Glu
XM_006718559.2:c.5916T>A	XP_006718622.1:p.Asp1972Glu
XM_006718560.2:c.5913T>A	XP_006718623.1:p.Asp1971Glu
XM_006718561.2:c.5916T>A	XP_006718624.1:p.Asp1972Glu
XM_011545044.1:c.6030T>A	XP_011543346.1:p.Asp2010Glu
XM_011545045.1:c.6024T>A	XP_011543347.1:p.Asp2008Glu
XM_011545046.1:c.5997T>A	XP_011543348.1:p.Asp1999Glu
XM_011545047.1:c.5934T>A	XP_011543349.1:p.Asp1978Glu
XM_011545048.1:c.5805T>A	XP_011543350.1:p.Asp1935Glu
XM_011545049.1:c.5793T>A	XP_011543351.1:p.Asp1931Glu
XM_011545050.1:c.5766T>A	XP_011543352.1:p.Asp1922Glu
XM_011545051.1:c.6030T>A	XP_011543353.1:p.Asp2010Glu
XR_949938.1:n.6350T>A
XR_949941.1:n.6324T>A
XM_011545044.2:c.6030T>A	XP_011543346.1:p.Asp2010Glu
XM_011545046.2:c.6120T>A	XP_011543348.2:p.Asp2040Glu
XM_011545050.2:c.5766T>A	XP_011543352.1:p.Asp1922Glu
XM_017017778.1:c.6114T>A	XP_016873267.1:p.Asp2038Glu
XM_017017779.1:c.6111T>A	XP_016873268.1:p.Asp2037Glu
XM_017017780.1:c.6120T>A	XP_016873269.1:p.Asp2040Glu
XM_017017781.1:c.6024T>A	XP_016873270.1:p.Asp2008Glu
XM_017017782.1:c.6006T>A	XP_016873271.1:p.Asp2002Glu
XM_017017783.1:c.6003T>A	XP_016873272.1:p.Asp2001Glu
XM_017017784.1:c.6003T>A	XP_016873273.1:p.Asp2001Glu
XM_017017785.1:c.5883T>A	XP_016873274.1:p.Asp1961Glu
XM_017017786.1:c.6120T>A	XP_016873275.1:p.Asp2040Glu
XM_017017788.1:c.6006T>A	XP_016873277.1:p.Asp2002Glu
XR_001747885.1:n.6109T>A
XR_001747886.1:n.6050T>A
XR_001747887.1:n.6095T>A
NM_000260.4:c.6030T>A MANE Select	NP_000251.3:p.Asp2010Glu
NM_001127180.2:c.5916T>A	NP_001120652.1:p.Asp1972Glu
NM_001369365.1:c.5883T>A	NP_001356294.1:p.Asp1961Glu