Canonical Allele Identifier: CA1143575197

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186095385T= , CM000663.2:g.186095385T=	GRCh38
NC_000001.10:g.186064517T= , CM000663.1:g.186064517T=	GRCh37
NC_000001.9:g.184331140T=	NCBI36
NG_011841.1:g.365835T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.10437T= MANE Select	ENSP00000271588.4:p.Asp3479=
ENST00000271588.8:c.10437T=	ENSP00000271588.4:p.Asp3479=
NM_031935.2:c.10437T=	NP_114141.2:p.Asp3479=
XM_011510037.1:c.10152T=	XP_011508339.1:p.Asp3384=
XM_011510038.1:c.10437T=	XP_011508340.1:p.Asp3479=
XM_011510039.1:c.10437T=	XP_011508341.1:p.Asp3479=
XM_011510040.1:c.*85T=	XP_011508342.1:n.*85T=
XM_011510038.3:c.10437T=	XP_011508340.1:p.Asp3479=
XM_017002437.1:c.8460T=	XP_016857926.1:p.Asp2820=
XM_024450118.1:c.*85T=	XP_024305886.1:n.*85T=
NM_031935.3:c.10437T= MANE Select	NP_114141.2:p.Asp3479=