Canonical Allele Identifier: CA2403834940

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36366589T= , CM000684.2:g.36366589T=	GRCh38
NC_000022.10:g.36762634T= , CM000684.1:g.36762634T=	GRCh37
NC_000022.9:g.35092580T=	NCBI36
NG_011884.2:g.26430A= , LRG_567:g.26430A=

Transcript Alleles

HGVS	Amino-acid Change
NM_002473.6:c.-19-17334A= MANE Select	NP_002464.1:n.-19-17334A=
ENST00000216181.11:c.-19-17334A= MANE Select	ENSP00000216181.6:n.-19-17334A=
NM_002473.5:c.-19-17334A= , LRG_567t1:c.-19-17334A=	NP_002464.1:n.-19-17334A=
ENST00000216181.9:c.-19-17334A=	ENSP00000216181.5:n.-19-17334A=
ENST00000685187.1:n.196-17334A=
ENST00000685191.1:n.205-17334A=
ENST00000685801.1:c.-19-17334A=	ENSP00000510688.1:n.-19-17334A=
ENST00000688137.1:c.-20+3997A=	ENSP00000510189.1:n.-20+3997A=
ENST00000691296.1:c.-19-17334A=	ENSP00000509816.1:n.-19-17334A=
ENST00000691687.1:n.196-17334A=
ENST00000692930.1:n.196-17334A=
XM_017028803.1:c.-19-17334A=	XP_016884292.1:n.-19-17334A=
XM_017028804.1:c.-20+3785A=	XP_016884293.1:n.-20+3785A=
XM_017028806.1:c.-19-17334A=	XP_016884295.1:n.-19-17334A=