Canonical Allele Identifier: CA2403794917

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36281937A= , CM000684.2:g.36281937A=	GRCh38
NC_000022.10:g.36677983A= , CM000684.1:g.36677983A=	GRCh37
NC_000022.9:g.35007929A=	NCBI36
NG_011884.2:g.111082T= , LRG_567:g.111082T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000685708.1:n.3047T=
ENST00000685801.1:c.*731T=	ENSP00000510688.1:n.*731T=
ENST00000690244.1:n.1950T=
ENST00000691109.1:n.6909T=
ENST00000216181.11:c.*731T= MANE Select	ENSP00000216181.6:n.*731T=
ENST00000216181.9:c.*731T=	ENSP00000216181.5:n.*731T=
NM_002473.5:c.*731T= , LRG_567t1:c.*731T=	NP_002464.1:n.*731T=
XM_011530197.1:c.*731T=	XP_011528499.1:n.*731T=
XM_011530197.2:c.*731T=	XP_011528499.1:n.*731T=
XM_017028803.1:c.*731T=	XP_016884292.1:n.*731T=
XM_017028804.1:c.*731T=	XP_016884293.1:n.*731T=
XM_017028805.1:c.*731T=	XP_016884294.1:n.*731T=
XM_017028806.1:c.*731T=	XP_016884295.1:n.*731T=
NM_002473.6:c.*731T= MANE Select	NP_002464.1:n.*731T=