Canonical Allele Identifier: CA1213027215

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186171956G= , CM000663.2:g.186171956G=	GRCh38
NC_000001.10:g.186141088G= , CM000663.1:g.186141088G=	GRCh37
NC_000001.9:g.184407711G=	NCBI36
NG_011841.1:g.442406G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.15689-50G= MANE Select	ENSP00000271588.4:n.15689-50G=
ENST00000271588.8:c.15689-50G=	ENSP00000271588.4:n.15689-50G=
ENST00000414277.1:c.65-50G=	ENSP00000406205.1:n.65-50G=
ENST00000475585.1:n.277-50G=
NM_031935.2:c.15689-50G=	NP_114141.2:n.15689-50G=
XM_011510037.1:c.15404-50G=	XP_011508339.1:n.15404-50G=
XM_011510038.1:c.15689-50G=	XP_011508340.1:n.15689-50G=
XM_011510038.3:c.15689-50G=	XP_011508340.1:n.15689-50G=
XM_017002437.1:c.13712-50G=	XP_016857926.1:n.13712-50G=
NM_031935.3:c.15689-50G= MANE Select	NP_114141.2:n.15689-50G=