Canonical Allele Identifier: CA1861285944
Gene: GOLM1 HGNC NCBI

Linked Data

dbSNP Id: rs1834692904

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86078644G>T , CM000671.2:g.86078644G>T GRCh38
NC_000009.11:g.88693559G>T , CM000671.1:g.88693559G>T GRCh37
NC_000009.10:g.87883379G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388711.7:c.129+548C>A ENSP00000373363.3:n.129+548C>A
ENST00000388712.7:c.129+548C>A MANE Select ENSP00000373364.3:n.129+548C>A
ENST00000466178.1:c.129+548C>A ENSP00000418155.1:n.129+548C>A
ENST00000470762.6:c.129+548C>A ENSP00000417504.2:n.129+548C>A
ENST00000472919.1:n.190+657C>A
ENST00000486130.5:c.129+548C>A ENSP00000419076.1:n.129+548C>A
NM_016548.3:c.129+548C>A NP_057632.2:n.129+548C>A
NM_177937.2:c.129+548C>A NP_808800.1:n.129+548C>A
NM_016548.4:c.129+548C>A MANE Select NP_057632.2:n.129+548C>A
NM_177937.3:c.129+548C>A NP_808800.1:n.129+548C>A