Canonical Allele Identifier: CA1139781074

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36281936G= , CM000684.2:g.36281936G=	GRCh38
NC_000022.10:g.36677982G= , CM000684.1:g.36677982G=	GRCh37
NC_000022.9:g.35007928G=	NCBI36
NG_011884.2:g.111083C= , LRG_567:g.111083C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000685708.1:n.3048C=
ENST00000685801.1:c.*732C=	ENSP00000510688.1:n.*732C=
ENST00000690244.1:n.1951C=
ENST00000691109.1:n.6910C=
ENST00000216181.11:c.*732C= MANE Select	ENSP00000216181.6:n.*732C=
ENST00000216181.9:c.*732C=	ENSP00000216181.5:n.*732C=
NM_002473.5:c.*732C= , LRG_567t1:c.*732C=	NP_002464.1:n.*732C=
XM_011530197.1:c.*732C=	XP_011528499.1:n.*732C=
XM_011530197.2:c.*732C=	XP_011528499.1:n.*732C=
XM_017028803.1:c.*732C=	XP_016884292.1:n.*732C=
XM_017028804.1:c.*732C=	XP_016884293.1:n.*732C=
XM_017028805.1:c.*732C=	XP_016884294.1:n.*732C=
XM_017028806.1:c.*732C=	XP_016884295.1:n.*732C=
NM_002473.6:c.*732C= MANE Select	NP_002464.1:n.*732C=