Canonical Allele Identifier: CA2403796196

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36284364G= , CM000684.2:g.36284364G=	GRCh38
NC_000022.10:g.36680410G= , CM000684.1:g.36680410G=	GRCh37
NC_000022.9:g.35010356G=	NCBI36
NG_011884.2:g.108655C= , LRG_567:g.108655C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2025+39C=
ENST00000685801.1:c.5655+39C=	ENSP00000510688.1:n.5655+39C=
ENST00000690244.1:n.928+39C=
ENST00000691109.1:n.5887+39C=
ENST00000216181.11:c.5592+39C= MANE Select	ENSP00000216181.6:n.5592+39C=
ENST00000216181.9:c.5592+39C=	ENSP00000216181.5:n.5592+39C=
ENST00000475726.5:n.622+39C=
ENST00000486218.1:n.638C=
NM_002473.5:c.5592+39C= , LRG_567t1:c.5592+39C=	NP_002464.1:n.5592+39C=
XM_011530197.1:c.5592+39C=	XP_011528499.1:n.5592+39C=
XM_011530197.2:c.5592+39C=	XP_011528499.1:n.5592+39C=
XM_017028803.1:c.5592+39C=	XP_016884292.1:n.5592+39C=
XM_017028804.1:c.5592+39C=	XP_016884293.1:n.5592+39C=
XM_017028805.1:c.5592+39C=	XP_016884294.1:n.5592+39C=
XM_017028806.1:c.5592+39C=	XP_016884295.1:n.5592+39C=
NM_002473.6:c.5592+39C= MANE Select	NP_002464.1:n.5592+39C=