Canonical Allele Identifier: CA1984131556

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77214692A= , CM000673.2:g.77214692A=	GRCh38
NC_000011.9:g.76925737A= , CM000673.1:g.76925737A=	GRCh37
NC_000011.8:g.76603385A=	NCBI36
NG_009086.1:g.91428A=
NG_009086.2:g.91447A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6644A= MANE Select	ENSP00000386331.3:p.Lys2215=
ENST00000670577.1:c.4445A=
ENST00000409619.6:c.6497A=	ENSP00000386635.2:p.Lys2166=
ENST00000409709.7:c.6644A=	ENSP00000386331.3:p.Lys2215=
ENST00000458169.2:c.4070A=	ENSP00000417017.2:p.Lys1357=
ENST00000458637.6:c.6524A=	ENSP00000392185.2:p.Lys2175=
ENST00000481328.7:n.5194A=
ENST00000605744.1:n.2158A=
NM_000260.3:c.6644A=	NP_000251.3:p.Lys2215=
NM_001127180.1:c.6524A=	NP_001120652.1:p.Lys2175=
XM_005274012.2:c.6527A=	XP_005274069.1:p.Lys2176=
XM_006718561.2:c.6530A=	XP_006718624.1:p.Lys2177=
XR_949941.1:n.6938A=
XM_017017780.1:c.6734A=	XP_016873269.1:p.Lys2245=
XM_017017784.1:c.6617A=	XP_016873273.1:p.Lys2206=
XM_017017788.1:c.6620A=	XP_016873277.1:p.Lys2207=
XR_001747885.1:n.6723A=
XR_001747887.1:n.6709A=
NM_000260.4:c.6644A= MANE Select	NP_000251.3:p.Lys2215=
NM_001127180.2:c.6524A=	NP_001120652.1:p.Lys2175=
NM_001369365.1:c.6497A=	NP_001356294.1:p.Lys2166=