Canonical Allele Identifier: CA343929731
Gene: HMCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186166807G>A , CM000663.2:g.186166807G>A GRCh38
NC_000001.10:g.186135939G>A , CM000663.1:g.186135939G>A GRCh37
NC_000001.9:g.184402562G>A NCBI36
NG_011841.1:g.437257G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271588.9:c.15440-1G>A MANE Select ENSP00000271588.4:n.15440-1G>A
ENST00000271588.8:c.15440-1G>A ENSP00000271588.4:n.15440-1G>A
ENST00000475585.1:n.163-4530G>A
NM_031935.2:c.15440-1G>A NP_114141.2:n.15440-1G>A
XM_011510037.1:c.15155-1G>A XP_011508339.1:n.15155-1G>A
XM_011510038.1:c.15440-1G>A XP_011508340.1:n.15440-1G>A
XM_011510038.3:c.15440-1G>A XP_011508340.1:n.15440-1G>A
XM_017002437.1:c.13463-1G>A XP_016857926.1:n.13463-1G>A
NM_031935.3:c.15440-1G>A MANE Select NP_114141.2:n.15440-1G>A