Canonical Allele Identifier: CA1213028289
Gene: HMCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186174425T= , CM000663.2:g.186174425T= GRCh38
NC_000001.10:g.186143557T= , CM000663.1:g.186143557T= GRCh37
NC_000001.9:g.184410180T= NCBI36
NG_011841.1:g.444875T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000271588.9:c.15815-89T= MANE Select ENSP00000271588.4:n.15815-89T=
ENST00000271588.8:c.15815-89T= ENSP00000271588.4:n.15815-89T=
ENST00000414277.1:c.191-89T= ENSP00000406205.1:n.191-89T=
NM_031935.2:c.15815-89T= NP_114141.2:n.15815-89T=
XM_011510037.1:c.15530-89T= XP_011508339.1:n.15530-89T=
XM_011510038.1:c.15815-89T= XP_011508340.1:n.15815-89T=
XM_011510038.3:c.15815-89T= XP_011508340.1:n.15815-89T=
XM_017002437.1:c.13838-89T= XP_016857926.1:n.13838-89T=
NM_031935.3:c.15815-89T= MANE Select NP_114141.2:n.15815-89T=