Canonical Allele Identifier: CA2403827088

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36350034G= , CM000684.2:g.36350034G=	GRCh38
NC_000022.10:g.36746079G= , CM000684.1:g.36746079G=	GRCh37
NC_000022.9:g.35076025G=	NCBI36
NG_011884.2:g.42985C= , LRG_567:g.42985C=

Transcript Alleles

HGVS	Amino-acid Change
NM_002473.6:c.-19-779C= MANE Select	NP_002464.1:n.-19-779C=
ENST00000216181.11:c.-19-779C= MANE Select	ENSP00000216181.6:n.-19-779C=
NM_002473.5:c.-19-779C= , LRG_567t1:c.-19-779C=	NP_002464.1:n.-19-779C=
ENST00000216181.9:c.-19-779C=	ENSP00000216181.5:n.-19-779C=
ENST00000401701.1:c.-19-779C=	ENSP00000384631.1:n.-19-779C=
ENST00000456729.1:c.-19-779C=	ENSP00000414852.1:n.-19-779C=
ENST00000685187.1:n.196-779C=
ENST00000685191.1:n.205-779C=
ENST00000685801.1:c.-19-779C=	ENSP00000510688.1:n.-19-779C=
ENST00000688137.1:c.-19-779C=	ENSP00000510189.1:n.-19-779C=
ENST00000691296.1:c.-19-779C=	ENSP00000509816.1:n.-19-779C=
ENST00000691687.1:n.196-779C=
ENST00000692930.1:n.196-779C=
XM_011530197.1:c.-19-779C=	XP_011528499.1:n.-19-779C=
XM_011530197.2:c.-19-779C=	XP_011528499.1:n.-19-779C=
XM_017028803.1:c.-19-779C=	XP_016884292.1:n.-19-779C=
XM_017028804.1:c.-19-779C=	XP_016884293.1:n.-19-779C=
XM_017028805.1:c.-19-779C=	XP_016884294.1:n.-19-779C=
XM_017028806.1:c.-19-779C=	XP_016884295.1:n.-19-779C=