Canonical Allele Identifier: CA1143360498

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186172060C= , CM000663.2:g.186172060C=	GRCh38
NC_000001.10:g.186141192C= , CM000663.1:g.186141192C=	GRCh37
NC_000001.9:g.184407815C=	NCBI36
NG_011841.1:g.442510C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.15743C= MANE Select	ENSP00000271588.4:p.Thr5248=
ENST00000271588.8:c.15743C=	ENSP00000271588.4:p.Thr5248=
ENST00000414277.1:c.119C=	ENSP00000406205.1:p.Thr40=
ENST00000475585.1:n.331C=
NM_031935.2:c.15743C=	NP_114141.2:p.Thr5248=
XM_011510037.1:c.15458C=	XP_011508339.1:p.Thr5153=
XM_011510038.1:c.15743C=	XP_011508340.1:p.Thr5248=
XM_011510038.3:c.15743C=	XP_011508340.1:p.Thr5248=
XM_017002437.1:c.13766C=	XP_016857926.1:p.Thr4589=
NM_031935.3:c.15743C= MANE Select	NP_114141.2:p.Thr5248=