Canonical Allele Identifier: CA195543751
Gene: GOLM1 HGNC NCBI

Linked Data

dbSNP Id: rs775274738
gnomAD v2: 9-88699827-G-A
gnomAD v3: 9-86084912-G-A
gnomAD v4: 9-86084912-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86084912G>A , CM000671.2:g.86084912G>A GRCh38
NC_000009.11:g.88699827G>A , CM000671.1:g.88699827G>A GRCh37
NC_000009.10:g.87889647G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388711.7:c.-21-5571C>T ENSP00000373363.3:n.-21-5571C>T
ENST00000388712.7:c.-21-5571C>T MANE Select ENSP00000373364.3:n.-21-5571C>T
ENST00000466178.1:c.-22+8C>T ENSP00000418155.1:n.-22+8C>T
ENST00000472919.1:n.150-5571C>T
NM_016548.3:c.-21-5571C>T NP_057632.2:n.-21-5571C>T
NM_177937.2:c.-21-5571C>T NP_808800.1:n.-21-5571C>T
NM_016548.4:c.-21-5571C>T MANE Select NP_057632.2:n.-21-5571C>T
NM_177937.3:c.-21-5571C>T NP_808800.1:n.-21-5571C>T