Canonical Allele Identifier: CA33468368

Gene: HMCN1

Linked Data

• dbSNP Id: rs577166967
• gnomAD v3: 1-186074774-G-A
• gnomAD v4: 1-186074774-G-A
• MyVariant Identifiers: chr1:g.186043906G>A (hg19) ; chr1:g.186074774G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186074774G>A , CM000663.2:g.186074774G>A	GRCh38
NC_000001.10:g.186043906G>A , CM000663.1:g.186043906G>A	GRCh37
NC_000001.9:g.184310529G>A	NCBI36
NG_011841.1:g.345224G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.8173G>A MANE Select	ENSP00000271588.4:p.Ala2725Thr
ENST00000271588.8:c.8173G>A	ENSP00000271588.4:p.Ala2725Thr
NM_031935.2:c.8173G>A	NP_114141.2:p.Ala2725Thr
XM_011510037.1:c.8173G>A	XP_011508339.1:p.Ala2725Thr
XM_011510038.1:c.8173G>A	XP_011508340.1:p.Ala2725Thr
XM_011510039.1:c.8173G>A	XP_011508341.1:p.Ala2725Thr
XM_011510040.1:c.8173G>A	XP_011508342.1:p.Ala2725Thr
XM_011510041.1:c.8173G>A	XP_011508343.1:p.Ala2725Thr
XM_011510038.3:c.8173G>A	XP_011508340.1:p.Ala2725Thr
XM_011510041.3:c.8173G>A	XP_011508343.1:p.Ala2725Thr
XM_017002437.1:c.6196G>A	XP_016857926.1:p.Ala2066Thr
XM_024450118.1:c.8173G>A	XP_024305886.1:p.Ala2725Thr
NM_031935.3:c.8173G>A MANE Select	NP_114141.2:p.Ala2725Thr