Canonical Allele Identifier: CA1861285700
Gene: GOLM1 HGNC NCBI

Linked Data

dbSNP Id: rs1834681567

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86078367G>A , CM000671.2:g.86078367G>A GRCh38
NC_000009.11:g.88693282G>A , CM000671.1:g.88693282G>A GRCh37
NC_000009.10:g.87883102G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388711.7:c.130-776C>T ENSP00000373363.3:n.130-776C>T
ENST00000388712.7:c.130-776C>T MANE Select ENSP00000373364.3:n.130-776C>T
ENST00000466178.1:c.130-776C>T ENSP00000418155.1:n.130-776C>T
ENST00000470762.6:c.130-776C>T ENSP00000417504.2:n.130-776C>T
ENST00000472919.1:n.191-828C>T
ENST00000486130.5:c.130-776C>T ENSP00000419076.1:n.130-776C>T
NM_016548.3:c.130-776C>T NP_057632.2:n.130-776C>T
NM_177937.2:c.130-776C>T NP_808800.1:n.130-776C>T
NM_016548.4:c.130-776C>T MANE Select NP_057632.2:n.130-776C>T
NM_177937.3:c.130-776C>T NP_808800.1:n.130-776C>T