Canonical Allele Identifier: CA1212995203

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186095395A= , CM000663.2:g.186095395A=	GRCh38
NC_000001.10:g.186064527A= , CM000663.1:g.186064527A=	GRCh37
NC_000001.9:g.184331150A=	NCBI36
NG_011841.1:g.365845A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.10447A= MANE Select	ENSP00000271588.4:p.Thr3483=
ENST00000271588.8:c.10447A=	ENSP00000271588.4:p.Thr3483=
NM_031935.2:c.10447A=	NP_114141.2:p.Thr3483=
XM_011510037.1:c.10162A=	XP_011508339.1:p.Thr3388=
XM_011510038.1:c.10447A=	XP_011508340.1:p.Thr3483=
XM_011510039.1:c.10447A=	XP_011508341.1:p.Thr3483=
XM_011510038.3:c.10447A=	XP_011508340.1:p.Thr3483=
XM_017002437.1:c.8470A=	XP_016857926.1:p.Thr2824=
XM_024450118.1:c.*95A=	XP_024305886.1:n.*95A=
NM_031935.3:c.10447A= MANE Select	NP_114141.2:p.Thr3483=