Canonical Allele Identifier: CA2403809527

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36312039C= , CM000684.2:g.36312039C=	GRCh38
NC_000022.10:g.36708084C= , CM000684.1:g.36708084C=	GRCh37
NC_000022.9:g.35038030C=	NCBI36
NG_011884.2:g.80980G= , LRG_567:g.80980G=

Transcript Alleles

HGVS	Amino-acid Change
NM_002473.6:c.1728+10G= MANE Select	NP_002464.1:n.1728+10G=
ENST00000216181.11:c.1728+10G= MANE Select	ENSP00000216181.6:n.1728+10G=
NM_002473.5:c.1728+10G= , LRG_567t1:c.1728+10G=	NP_002464.1:n.1728+10G=
ENST00000216181.9:c.1728+10G=	ENSP00000216181.5:n.1728+10G=
ENST00000685187.1:n.1952G=
ENST00000685801.1:c.1728+10G=	ENSP00000510688.1:n.1728+10G=
ENST00000691109.1:n.2023+10G=
ENST00000691687.1:n.2536G=
ENST00000692930.1:n.1942+10G=
XM_011530197.1:c.1728+10G=	XP_011528499.1:n.1728+10G=
XM_011530197.2:c.1728+10G=	XP_011528499.1:n.1728+10G=
XM_017028803.1:c.1728+10G=	XP_016884292.1:n.1728+10G=
XM_017028804.1:c.1728+10G=	XP_016884293.1:n.1728+10G=
XM_017028805.1:c.1728+10G=	XP_016884294.1:n.1728+10G=
XM_017028806.1:c.1728+10G=	XP_016884295.1:n.1728+10G=