Canonical Allele Identifier: CA2649561974
Gene: HMCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186174427G>C , CM000663.2:g.186174427G>C GRCh38
NC_000001.10:g.186143559G>C , CM000663.1:g.186143559G>C GRCh37
NC_000001.9:g.184410182G>C NCBI36
NG_011841.1:g.444877G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000271588.9:c.15815-87G>C MANE Select ENSP00000271588.4:n.15815-87G>C
ENST00000271588.8:c.15815-87G>C ENSP00000271588.4:n.15815-87G>C
ENST00000414277.1:c.191-87G>C ENSP00000406205.1:n.191-87G>C
NM_031935.2:c.15815-87G>C NP_114141.2:n.15815-87G>C
XM_011510037.1:c.15530-87G>C XP_011508339.1:n.15530-87G>C
XM_011510038.1:c.15815-87G>C XP_011508340.1:n.15815-87G>C
XM_011510038.3:c.15815-87G>C XP_011508340.1:n.15815-87G>C
XM_017002437.1:c.13838-87G>C XP_016857926.1:n.13838-87G>C
NM_031935.3:c.15815-87G>C MANE Select NP_114141.2:n.15815-87G>C