Canonical Allele Identifier: CA1144969743

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186172062C= , CM000663.2:g.186172062C=	GRCh38
NC_000001.10:g.186141194C= , CM000663.1:g.186141194C=	GRCh37
NC_000001.9:g.184407817C=	NCBI36
NG_011841.1:g.442512C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.15745C= MANE Select	ENSP00000271588.4:p.Arg5249=
ENST00000271588.8:c.15745C=	ENSP00000271588.4:p.Arg5249=
ENST00000414277.1:c.121C=	ENSP00000406205.1:p.Arg41=
ENST00000475585.1:n.333C=
NM_031935.2:c.15745C=	NP_114141.2:p.Arg5249=
XM_011510037.1:c.15460C=	XP_011508339.1:p.Arg5154=
XM_011510038.1:c.15745C=	XP_011508340.1:p.Arg5249=
XM_011510038.3:c.15745C=	XP_011508340.1:p.Arg5249=
XM_017002437.1:c.13768C=	XP_016857926.1:p.Arg4590=
NM_031935.3:c.15745C= MANE Select	NP_114141.2:p.Arg5249=