Canonical Allele Identifier: CA1984127846

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77207294C= , CM000673.2:g.77207294C=	GRCh38
NC_000011.9:g.76918339C= , CM000673.1:g.76918339C=	GRCh37
NC_000011.8:g.76595987C=	NCBI36
NG_009086.1:g.84030C=
NG_009086.2:g.84049C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.5748C= MANE Select	ENSP00000386331.3:p.Phe1916=
ENST00000670577.1:c.3575C=
ENST00000409619.6:c.5601C=	ENSP00000386635.2:p.Phe1867=
ENST00000409709.7:c.5748C=	ENSP00000386331.3:p.Phe1916=
ENST00000458169.2:c.3174C=	ENSP00000417017.2:p.Phe1058=
ENST00000458637.6:c.5634C=	ENSP00000392185.2:p.Phe1878=
ENST00000481328.7:n.3284C=
ENST00000605744.1:n.662C=
NM_000260.3:c.5748C=	NP_000251.3:p.Phe1916=
NM_001127180.1:c.5634C=	NP_001120652.1:p.Phe1878=
XM_005274012.2:c.5631C=	XP_005274069.1:p.Phe1877=
XM_006718558.2:c.5739C=	XP_006718621.1:p.Phe1913=
XM_006718559.2:c.5634C=	XP_006718622.1:p.Phe1878=
XM_006718560.2:c.5631C=	XP_006718623.1:p.Phe1877=
XM_006718561.2:c.5634C=	XP_006718624.1:p.Phe1878=
XM_011545044.1:c.5748C=	XP_011543346.1:p.Phe1916=
XM_011545045.1:c.5742C=	XP_011543347.1:p.Phe1914=
XM_011545046.1:c.5715C=	XP_011543348.1:p.Phe1905=
XM_011545047.1:c.5652C=	XP_011543349.1:p.Phe1884=
XM_011545048.1:c.5523C=	XP_011543350.1:p.Phe1841=
XM_011545049.1:c.5511C=	XP_011543351.1:p.Phe1837=
XM_011545050.1:c.5484C=	XP_011543352.1:p.Phe1828=
XM_011545051.1:c.5748C=	XP_011543353.1:p.Phe1916=
XR_949938.1:n.6068C=
XR_949941.1:n.6068C=
XM_011545044.2:c.5748C=	XP_011543346.1:p.Phe1916=
XM_011545046.2:c.5838C=	XP_011543348.2:p.Phe1946=
XM_011545050.2:c.5484C=	XP_011543352.1:p.Phe1828=
XM_017017778.1:c.5832C=	XP_016873267.1:p.Phe1944=
XM_017017779.1:c.5829C=	XP_016873268.1:p.Phe1943=
XM_017017780.1:c.5838C=	XP_016873269.1:p.Phe1946=
XM_017017781.1:c.5742C=	XP_016873270.1:p.Phe1914=
XM_017017782.1:c.5724C=	XP_016873271.1:p.Phe1908=
XM_017017783.1:c.5721C=	XP_016873272.1:p.Phe1907=
XM_017017784.1:c.5721C=	XP_016873273.1:p.Phe1907=
XM_017017785.1:c.5601C=	XP_016873274.1:p.Phe1867=
XM_017017786.1:c.5838C=	XP_016873275.1:p.Phe1946=
XM_017017788.1:c.5724C=	XP_016873277.1:p.Phe1908=
XR_001747885.1:n.5853C=
XR_001747886.1:n.5768C=
XR_001747887.1:n.5839C=
NM_000260.4:c.5748C= MANE Select	NP_000251.3:p.Phe1916=
NM_001127180.2:c.5634C=	NP_001120652.1:p.Phe1878=
NM_001369365.1:c.5601C=	NP_001356294.1:p.Phe1867=