Canonical Allele Identifier: CA1212995202

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186095390A= , CM000663.2:g.186095390A=	GRCh38
NC_000001.10:g.186064522A= , CM000663.1:g.186064522A=	GRCh37
NC_000001.9:g.184331145A=	NCBI36
NG_011841.1:g.365840A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.10442A= MANE Select	ENSP00000271588.4:p.His3481=
ENST00000271588.8:c.10442A=	ENSP00000271588.4:p.His3481=
NM_031935.2:c.10442A=	NP_114141.2:p.His3481=
XM_011510037.1:c.10157A=	XP_011508339.1:p.His3386=
XM_011510038.1:c.10442A=	XP_011508340.1:p.His3481=
XM_011510039.1:c.10442A=	XP_011508341.1:p.His3481=
XM_011510038.3:c.10442A=	XP_011508340.1:p.His3481=
XM_017002437.1:c.8465A=	XP_016857926.1:p.His2822=
XM_024450118.1:c.*90A=	XP_024305886.1:n.*90A=
NM_031935.3:c.10442A= MANE Select	NP_114141.2:p.His3481=