Canonical Allele Identifier: CA1212950870

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.185993130G= , CM000663.2:g.185993130G=	GRCh38
NC_000001.10:g.185962262G= , CM000663.1:g.185962262G=	GRCh37
NC_000001.9:g.184228885G=	NCBI36
NG_011841.1:g.263580G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000271588.9:c.3378-52G= MANE Select	ENSP00000271588.4:n.3378-52G=
ENST00000271588.8:c.3378-52G=	ENSP00000271588.4:n.3378-52G=
ENST00000485744.5:n.1629-52G=
NM_031935.2:c.3378-52G=	NP_114141.2:n.3378-52G=
XM_011510037.1:c.3378-52G=	XP_011508339.1:n.3378-52G=
XM_011510038.1:c.3378-52G=	XP_011508340.1:n.3378-52G=
XM_011510039.1:c.3378-52G=	XP_011508341.1:n.3378-52G=
XM_011510040.1:c.3378-52G=	XP_011508342.1:n.3378-52G=
XM_011510041.1:c.3378-52G=	XP_011508343.1:n.3378-52G=
XM_011510038.3:c.3378-52G=	XP_011508340.1:n.3378-52G=
XM_011510041.3:c.3378-52G=	XP_011508343.1:n.3378-52G=
XM_017002437.1:c.1401-52G=	XP_016857926.1:n.1401-52G=
XM_024450118.1:c.3378-52G=	XP_024305886.1:n.3378-52G=
NM_031935.3:c.3378-52G= MANE Select	NP_114141.2:n.3378-52G=