Canonical Allele Identifier: CA343931392

Gene: HMCN1

Linked Data

• MyVariant Identifiers: chr1:g.186064617G>C (hg19) ; chr1:g.186095485G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186095485G>C , CM000663.2:g.186095485G>C	GRCh38
NC_000001.10:g.186064617G>C , CM000663.1:g.186064617G>C	GRCh37
NC_000001.9:g.184331240G>C	NCBI36
NG_011841.1:g.365935G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.10537G>C MANE Select	ENSP00000271588.4:p.Gly3513Arg
ENST00000271588.8:c.10537G>C	ENSP00000271588.4:p.Gly3513Arg
NM_031935.2:c.10537G>C	NP_114141.2:p.Gly3513Arg
XM_011510037.1:c.10252G>C	XP_011508339.1:p.Gly3418Arg
XM_011510038.1:c.10537G>C	XP_011508340.1:p.Gly3513Arg
XM_011510039.1:c.10537G>C	XP_011508341.1:p.Gly3513Arg
XM_011510038.3:c.10537G>C	XP_011508340.1:p.Gly3513Arg
XM_017002437.1:c.8560G>C	XP_016857926.1:p.Gly2854Arg
NM_031935.3:c.10537G>C MANE Select	NP_114141.2:p.Gly3513Arg