Canonical Allele Identifier: CA867920588
Gene: GOLM1 HGNC NCBI

Linked Data

dbSNP Id: rs1402305660
gnomAD v3: 9-86085087-T-A
gnomAD v4: 9-86085087-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86085087T>A , CM000671.2:g.86085087T>A GRCh38
NC_000009.11:g.88700002T>A , CM000671.1:g.88700002T>A GRCh37
NC_000009.10:g.87889822T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000388711.7:c.-21-5746A>T ENSP00000373363.3:n.-21-5746A>T
ENST00000388712.7:c.-21-5746A>T MANE Select ENSP00000373364.3:n.-21-5746A>T
ENST00000466178.1:c.-141-48A>T ENSP00000418155.1:n.-141-48A>T
ENST00000472919.1:n.150-5746A>T
NM_016548.3:c.-21-5746A>T NP_057632.2:n.-21-5746A>T
NM_177937.2:c.-21-5746A>T NP_808800.1:n.-21-5746A>T
NM_016548.4:c.-21-5746A>T MANE Select NP_057632.2:n.-21-5746A>T
NM_177937.3:c.-21-5746A>T NP_808800.1:n.-21-5746A>T