Canonical Allele Identifier: CA2403795024

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282125G= , CM000684.2:g.36282125G=	GRCh38
NC_000022.10:g.36678171G= , CM000684.1:g.36678171G=	GRCh37
NC_000022.9:g.35008117G=	NCBI36
NG_011884.2:g.110894C= , LRG_567:g.110894C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2859C=
ENST00000685801.1:c.*543C=	ENSP00000510688.1:n.*543C=
ENST00000690244.1:n.1762C=
ENST00000691109.1:n.6721C=
ENST00000216181.11:c.*543C= MANE Select	ENSP00000216181.6:n.*543C=
ENST00000216181.9:c.*543C=	ENSP00000216181.5:n.*543C=
NM_002473.5:c.*543C= , LRG_567t1:c.*543C=	NP_002464.1:n.*543C=
XM_011530197.1:c.*543C=	XP_011528499.1:n.*543C=
XM_011530197.2:c.*543C=	XP_011528499.1:n.*543C=
XM_017028803.1:c.*543C=	XP_016884292.1:n.*543C=
XM_017028804.1:c.*543C=	XP_016884293.1:n.*543C=
XM_017028805.1:c.*543C=	XP_016884294.1:n.*543C=
XM_017028806.1:c.*543C=	XP_016884295.1:n.*543C=
NM_002473.6:c.*543C= MANE Select	NP_002464.1:n.*543C=