Canonical Allele Identifier: CA2403811698

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36316686G= , CM000684.2:g.36316686G=	GRCh38
NC_000022.10:g.36712731G= , CM000684.1:g.36712731G=	GRCh37
NC_000022.9:g.35042677G=	NCBI36
NG_011884.2:g.76333C= , LRG_567:g.76333C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685187.1:n.1442-17C=
ENST00000685801.1:c.1228-17C=	ENSP00000510688.1:n.1228-17C=
ENST00000691109.1:n.1523-17C=
ENST00000691687.1:n.2026-17C=
ENST00000692930.1:n.1442-17C=
ENST00000216181.11:c.1228-17C= MANE Select	ENSP00000216181.6:n.1228-17C=
ENST00000216181.9:c.1228-17C=	ENSP00000216181.5:n.1228-17C=
ENST00000477189.1:n.416-17C=
NM_002473.5:c.1228-17C= , LRG_567t1:c.1228-17C=	NP_002464.1:n.1228-17C=
XM_011530197.1:c.1228-17C=	XP_011528499.1:n.1228-17C=
XM_011530197.2:c.1228-17C=	XP_011528499.1:n.1228-17C=
XM_017028803.1:c.1228-17C=	XP_016884292.1:n.1228-17C=
XM_017028804.1:c.1228-17C=	XP_016884293.1:n.1228-17C=
XM_017028805.1:c.1228-17C=	XP_016884294.1:n.1228-17C=
XM_017028806.1:c.1228-17C=	XP_016884295.1:n.1228-17C=
NM_002473.6:c.1228-17C= MANE Select	NP_002464.1:n.1228-17C=