Canonical Allele Identifier: CA1861285840
Gene: GOLM1 HGNC NCBI

Linked Data

dbSNP Id: rs1834688123

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86078503T>A , CM000671.2:g.86078503T>A GRCh38
NC_000009.11:g.88693418T>A , CM000671.1:g.88693418T>A GRCh37
NC_000009.10:g.87883238T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000388711.7:c.129+689A>T ENSP00000373363.3:n.129+689A>T
ENST00000388712.7:c.129+689A>T MANE Select ENSP00000373364.3:n.129+689A>T
ENST00000466178.1:c.129+689A>T ENSP00000418155.1:n.129+689A>T
ENST00000470762.6:c.129+689A>T ENSP00000417504.2:n.129+689A>T
ENST00000472919.1:n.190+798A>T
ENST00000486130.5:c.129+689A>T ENSP00000419076.1:n.129+689A>T
NM_016548.3:c.129+689A>T NP_057632.2:n.129+689A>T
NM_177937.2:c.129+689A>T NP_808800.1:n.129+689A>T
NM_016548.4:c.129+689A>T MANE Select NP_057632.2:n.129+689A>T
NM_177937.3:c.129+689A>T NP_808800.1:n.129+689A>T