Canonical Allele Identifier: CA1212957654

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186003711G= , CM000663.2:g.186003711G=	GRCh38
NC_000001.10:g.185972843G= , CM000663.1:g.185972843G=	GRCh37
NC_000001.9:g.184239466G=	NCBI36
NG_011841.1:g.274161G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.4349-7G= MANE Select	ENSP00000271588.4:n.4349-7G=
ENST00000271588.8:c.4349-7G=	ENSP00000271588.4:n.4349-7G=
NM_031935.2:c.4349-7G=	NP_114141.2:n.4349-7G=
XM_011510037.1:c.4349-7G=	XP_011508339.1:n.4349-7G=
XM_011510038.1:c.4349-7G=	XP_011508340.1:n.4349-7G=
XM_011510039.1:c.4349-7G=	XP_011508341.1:n.4349-7G=
XM_011510040.1:c.4349-7G=	XP_011508342.1:n.4349-7G=
XM_011510041.1:c.4349-7G=	XP_011508343.1:n.4349-7G=
XM_011510038.3:c.4349-7G=	XP_011508340.1:n.4349-7G=
XM_011510041.3:c.4349-7G=	XP_011508343.1:n.4349-7G=
XM_017002437.1:c.2372-7G=	XP_016857926.1:n.2372-7G=
XM_024450118.1:c.4349-7G=	XP_024305886.1:n.4349-7G=
NM_031935.3:c.4349-7G= MANE Select	NP_114141.2:n.4349-7G=