Canonical Allele Identifier: CA1213027254

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186172053A= , CM000663.2:g.186172053A=	GRCh38
NC_000001.10:g.186141185A= , CM000663.1:g.186141185A=	GRCh37
NC_000001.9:g.184407808A=	NCBI36
NG_011841.1:g.442503A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.15736A= MANE Select	ENSP00000271588.4:p.Lys5246=
ENST00000271588.8:c.15736A=	ENSP00000271588.4:p.Lys5246=
ENST00000414277.1:c.112A=	ENSP00000406205.1:p.Lys38=
ENST00000475585.1:n.324A=
NM_031935.2:c.15736A=	NP_114141.2:p.Lys5246=
XM_011510037.1:c.15451A=	XP_011508339.1:p.Lys5151=
XM_011510038.1:c.15736A=	XP_011508340.1:p.Lys5246=
XM_011510038.3:c.15736A=	XP_011508340.1:p.Lys5246=
XM_017002437.1:c.13759A=	XP_016857926.1:p.Lys4587=
NM_031935.3:c.15736A= MANE Select	NP_114141.2:p.Lys5246=