Canonical Allele Identifier: CA2403814609

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36322813G= , CM000684.2:g.36322813G=	GRCh38
NC_000022.10:g.36718858G= , CM000684.1:g.36718858G=	GRCh37
NC_000022.9:g.35048804G=	NCBI36
NG_011884.2:g.70206C= , LRG_567:g.70206C=

Transcript Alleles

HGVS	Amino-acid Change
NM_002473.6:c.613-292C= MANE Select	NP_002464.1:n.613-292C=
ENST00000216181.11:c.613-292C= MANE Select	ENSP00000216181.6:n.613-292C=
NM_002473.5:c.613-292C= , LRG_567t1:c.613-292C=	NP_002464.1:n.613-292C=
ENST00000216181.9:c.613-292C=	ENSP00000216181.5:n.613-292C=
ENST00000463027.1:n.217-292C=
ENST00000685187.1:n.827-292C=
ENST00000685191.1:n.836-292C=
ENST00000685801.1:c.613-292C=	ENSP00000510688.1:n.613-292C=
ENST00000691109.1:n.182C=
ENST00000691687.1:n.827-292C=
ENST00000692930.1:n.827-292C=
XM_011530197.1:c.613-292C=	XP_011528499.1:n.613-292C=
XM_011530197.2:c.613-292C=	XP_011528499.1:n.613-292C=
XM_017028803.1:c.613-292C=	XP_016884292.1:n.613-292C=
XM_017028804.1:c.613-292C=	XP_016884293.1:n.613-292C=
XM_017028805.1:c.613-292C=	XP_016884294.1:n.613-292C=
XM_017028806.1:c.613-292C=	XP_016884295.1:n.613-292C=