Canonical Allele Identifier: CA2403811662

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36316596T= , CM000684.2:g.36316596T=	GRCh38
NC_000022.10:g.36712641T= , CM000684.1:g.36712641T=	GRCh37
NC_000022.9:g.35042587T=	NCBI36
NG_011884.2:g.76423A= , LRG_567:g.76423A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685187.1:n.1515A=
ENST00000685801.1:c.1301A=	ENSP00000510688.1:p.Asn434=
ENST00000691109.1:n.1596A=
ENST00000691687.1:n.2099A=
ENST00000692930.1:n.1515A=
ENST00000216181.11:c.1301A= MANE Select	ENSP00000216181.6:p.Asn434=
ENST00000216181.9:c.1301A=	ENSP00000216181.5:p.Asn434=
ENST00000477189.1:n.489A=
NM_002473.5:c.1301A= , LRG_567t1:c.1301A=	NP_002464.1:p.Asn434=
XM_011530197.1:c.1301A=	XP_011528499.1:p.Asn434=
XM_011530197.2:c.1301A=	XP_011528499.1:p.Asn434=
XM_017028803.1:c.1301A=	XP_016884292.1:p.Asn434=
XM_017028804.1:c.1301A=	XP_016884293.1:p.Asn434=
XM_017028805.1:c.1301A=	XP_016884294.1:p.Asn434=
XM_017028806.1:c.1301A=	XP_016884295.1:p.Asn434=
NM_002473.6:c.1301A= MANE Select	NP_002464.1:p.Asn434=