Canonical Allele Identifier: CA3084787734

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186172055G= , CM000663.2:g.186172055G=	GRCh38
NC_000001.10:g.186141187G= , CM000663.1:g.186141187G=	GRCh37
NC_000001.9:g.184407810G=	NCBI36
NG_011841.1:g.442505G=

Transcript Alleles

HGVS	Amino-acid Change
NM_031935.3:c.15738G= MANE Select	NP_114141.2:p.Lys5246=
ENST00000271588.9:c.15738G= MANE Select	ENSP00000271588.4:p.Lys5246=
NM_031935.2:c.15738G=	NP_114141.2:p.Lys5246=
ENST00000271588.8:c.15738G=	ENSP00000271588.4:p.Lys5246=
ENST00000414277.1:c.114G=	ENSP00000406205.1:p.Lys38=
ENST00000475585.1:n.326G=
XM_011510037.1:c.15453G=	XP_011508339.1:p.Lys5151=
XM_011510038.1:c.15738G=	XP_011508340.1:p.Lys5246=
XM_011510038.3:c.15738G=	XP_011508340.1:p.Lys5246=
XM_017002437.1:c.13761G=	XP_016857926.1:p.Lys4587=