Canonical Allele Identifier: CA1213027256
Gene: HMCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186172061C= , CM000663.2:g.186172061C= GRCh38
NC_000001.10:g.186141193C= , CM000663.1:g.186141193C= GRCh37
NC_000001.9:g.184407816C= NCBI36
NG_011841.1:g.442511C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000271588.9:c.15744C= MANE Select ENSP00000271588.4:p.Thr5248=
ENST00000271588.8:c.15744C= ENSP00000271588.4:p.Thr5248=
ENST00000414277.1:c.120C= ENSP00000406205.1:p.Thr40=
ENST00000475585.1:n.332C=
NM_031935.2:c.15744C= NP_114141.2:p.Thr5248=
XM_011510037.1:c.15459C= XP_011508339.1:p.Thr5153=
XM_011510038.1:c.15744C= XP_011508340.1:p.Thr5248=
XM_011510038.3:c.15744C= XP_011508340.1:p.Thr5248=
XM_017002437.1:c.13767C= XP_016857926.1:p.Thr4589=
NM_031935.3:c.15744C= MANE Select NP_114141.2:p.Thr5248=