Canonical Allele Identifier: CA2403796226

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36284428C= , CM000684.2:g.36284428C=	GRCh38
NC_000022.10:g.36680474C= , CM000684.1:g.36680474C=	GRCh37
NC_000022.9:g.35010420C=	NCBI36
NG_011884.2:g.108591G= , LRG_567:g.108591G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2000G=
ENST00000685801.1:c.5630G=	ENSP00000510688.1:p.Arg1877=
ENST00000690244.1:n.903G=
ENST00000691109.1:n.5862G=
ENST00000216181.11:c.5567G= MANE Select	ENSP00000216181.6:p.Arg1856=
ENST00000216181.9:c.5567G=	ENSP00000216181.5:p.Arg1856=
ENST00000475726.5:n.597G=
ENST00000486218.1:n.574G=
NM_002473.5:c.5567G= , LRG_567t1:c.5567G=	NP_002464.1:p.Arg1856=
XM_011530197.1:c.5567G=	XP_011528499.1:p.Arg1856=
XM_011530197.2:c.5567G=	XP_011528499.1:p.Arg1856=
XM_017028803.1:c.5567G=	XP_016884292.1:p.Arg1856=
XM_017028804.1:c.5567G=	XP_016884293.1:p.Arg1856=
XM_017028805.1:c.5567G=	XP_016884294.1:p.Arg1856=
XM_017028806.1:c.5567G=	XP_016884295.1:p.Arg1856=
NM_002473.6:c.5567G= MANE Select	NP_002464.1:p.Arg1856=