Canonical Allele Identifier: CA2403811686

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36316654C= , CM000684.2:g.36316654C=	GRCh38
NC_000022.10:g.36712699C= , CM000684.1:g.36712699C=	GRCh37
NC_000022.9:g.35042645C=	NCBI36
NG_011884.2:g.76365G= , LRG_567:g.76365G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685187.1:n.1457G=
ENST00000685801.1:c.1243G=	ENSP00000510688.1:p.Glu415=
ENST00000691109.1:n.1538G=
ENST00000691687.1:n.2041G=
ENST00000692930.1:n.1457G=
ENST00000216181.11:c.1243G= MANE Select	ENSP00000216181.6:p.Glu415=
ENST00000216181.9:c.1243G=	ENSP00000216181.5:p.Glu415=
ENST00000477189.1:n.431G=
NM_002473.5:c.1243G= , LRG_567t1:c.1243G=	NP_002464.1:p.Glu415=
XM_011530197.1:c.1243G=	XP_011528499.1:p.Glu415=
XM_011530197.2:c.1243G=	XP_011528499.1:p.Glu415=
XM_017028803.1:c.1243G=	XP_016884292.1:p.Glu415=
XM_017028804.1:c.1243G=	XP_016884293.1:p.Glu415=
XM_017028805.1:c.1243G=	XP_016884294.1:p.Glu415=
XM_017028806.1:c.1243G=	XP_016884295.1:p.Glu415=
NM_002473.6:c.1243G= MANE Select	NP_002464.1:p.Glu415=