Canonical Allele Identifier: CA1212950891

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.185993146T= , CM000663.2:g.185993146T=	GRCh38
NC_000001.10:g.185962278T= , CM000663.1:g.185962278T=	GRCh37
NC_000001.9:g.184228901T=	NCBI36
NG_011841.1:g.263596T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000271588.9:c.3378-36T= MANE Select	ENSP00000271588.4:n.3378-36T=
ENST00000271588.8:c.3378-36T=	ENSP00000271588.4:n.3378-36T=
ENST00000485744.5:n.1629-36T=
NM_031935.2:c.3378-36T=	NP_114141.2:n.3378-36T=
XM_011510037.1:c.3378-36T=	XP_011508339.1:n.3378-36T=
XM_011510038.1:c.3378-36T=	XP_011508340.1:n.3378-36T=
XM_011510039.1:c.3378-36T=	XP_011508341.1:n.3378-36T=
XM_011510040.1:c.3378-36T=	XP_011508342.1:n.3378-36T=
XM_011510041.1:c.3378-36T=	XP_011508343.1:n.3378-36T=
XM_011510038.3:c.3378-36T=	XP_011508340.1:n.3378-36T=
XM_011510041.3:c.3378-36T=	XP_011508343.1:n.3378-36T=
XM_017002437.1:c.1401-36T=	XP_016857926.1:n.1401-36T=
XM_024450118.1:c.3378-36T=	XP_024305886.1:n.3378-36T=
NM_031935.3:c.3378-36T= MANE Select	NP_114141.2:n.3378-36T=