Canonical Allele Identifier: CA2403795029

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282139G= , CM000684.2:g.36282139G=	GRCh38
NC_000022.10:g.36678185G= , CM000684.1:g.36678185G=	GRCh37
NC_000022.9:g.35008131G=	NCBI36
NG_011884.2:g.110880C= , LRG_567:g.110880C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2845C=
ENST00000685801.1:c.*529C=	ENSP00000510688.1:n.*529C=
ENST00000690244.1:n.1748C=
ENST00000691109.1:n.6707C=
ENST00000216181.11:c.*529C= MANE Select	ENSP00000216181.6:n.*529C=
ENST00000216181.9:c.*529C=	ENSP00000216181.5:n.*529C=
NM_002473.5:c.*529C= , LRG_567t1:c.*529C=	NP_002464.1:n.*529C=
XM_011530197.1:c.*529C=	XP_011528499.1:n.*529C=
XM_011530197.2:c.*529C=	XP_011528499.1:n.*529C=
XM_017028803.1:c.*529C=	XP_016884292.1:n.*529C=
XM_017028804.1:c.*529C=	XP_016884293.1:n.*529C=
XM_017028805.1:c.*529C=	XP_016884294.1:n.*529C=
XM_017028806.1:c.*529C=	XP_016884295.1:n.*529C=
NM_002473.6:c.*529C= MANE Select	NP_002464.1:n.*529C=