Canonical Allele Identifier: CA1212846635

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.185734740T= , CM000663.2:g.185734740T=	GRCh38
NC_000001.10:g.185703872T= , CM000663.1:g.185703872T=	GRCh37
NC_000001.9:g.183970495T=	NCBI36
NG_011841.1:g.5190T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.-40T= MANE Select	ENSP00000271588.4:n.-40T=
ENST00000271588.8:c.-40T=	ENSP00000271588.4:n.-40T=
NM_031935.2:c.-40T=	NP_114141.2:n.-40T=
XM_011510037.1:c.-40T=	XP_011508339.1:n.-40T=
XM_011510038.1:c.-40T=	XP_011508340.1:n.-40T=
XM_011510039.1:c.-40T=	XP_011508341.1:n.-40T=
XM_011510040.1:c.-40T=	XP_011508342.1:n.-40T=
XM_011510041.1:c.-40T=	XP_011508343.1:n.-40T=
XM_011510038.3:c.-40T=	XP_011508340.1:n.-40T=
XM_011510041.3:c.-40T=	XP_011508343.1:n.-40T=
XM_024450118.1:c.-40T=	XP_024305886.1:n.-40T=
NM_031935.3:c.-40T= MANE Select	NP_114141.2:n.-40T=