Canonical Allele Identifier: CA1295289
Gene: HMCN1 HGNC NCBI

Linked Data

dbSNP Id: rs780687562

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186166901G>A , CM000663.2:g.186166901G>A GRCh38
NC_000001.10:g.186136033G>A , CM000663.1:g.186136033G>A GRCh37
NC_000001.9:g.184402656G>A NCBI36
NG_011841.1:g.437351G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271588.9:c.15533G>A MANE Select ENSP00000271588.4:p.Gly5178Glu
ENST00000271588.8:c.15533G>A ENSP00000271588.4:p.Gly5178Glu
ENST00000475585.1:n.163-4436G>A
NM_031935.2:c.15533G>A NP_114141.2:p.Gly5178Glu
XM_011510037.1:c.15248G>A XP_011508339.1:p.Gly5083Glu
XM_011510038.1:c.15533G>A XP_011508340.1:p.Gly5178Glu
XM_011510038.3:c.15533G>A XP_011508340.1:p.Gly5178Glu
XM_017002437.1:c.13556G>A XP_016857926.1:p.Gly4519Glu
NM_031935.3:c.15533G>A MANE Select NP_114141.2:p.Gly5178Glu