Canonical Allele Identifier: CA2403796225

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36284425T= , CM000684.2:g.36284425T=	GRCh38
NC_000022.10:g.36680471T= , CM000684.1:g.36680471T=	GRCh37
NC_000022.9:g.35010417T=	NCBI36
NG_011884.2:g.108594A= , LRG_567:g.108594A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2003A=
ENST00000685801.1:c.5633A=	ENSP00000510688.1:p.Asn1878=
ENST00000690244.1:n.906A=
ENST00000691109.1:n.5865A=
ENST00000216181.11:c.5570A= MANE Select	ENSP00000216181.6:p.Asn1857=
ENST00000216181.9:c.5570A=	ENSP00000216181.5:p.Asn1857=
ENST00000475726.5:n.600A=
ENST00000486218.1:n.577A=
NM_002473.5:c.5570A= , LRG_567t1:c.5570A=	NP_002464.1:p.Asn1857=
XM_011530197.1:c.5570A=	XP_011528499.1:p.Asn1857=
XM_011530197.2:c.5570A=	XP_011528499.1:p.Asn1857=
XM_017028803.1:c.5570A=	XP_016884292.1:p.Asn1857=
XM_017028804.1:c.5570A=	XP_016884293.1:p.Asn1857=
XM_017028805.1:c.5570A=	XP_016884294.1:p.Asn1857=
XM_017028806.1:c.5570A=	XP_016884295.1:p.Asn1857=
NM_002473.6:c.5570A= MANE Select	NP_002464.1:p.Asn1857=