Canonical Allele Identifier: CA2512431548
Gene: GOLM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86078037G>T , CM000671.2:g.86078037G>T GRCh38
NC_000009.11:g.88692952G>T , CM000671.1:g.88692952G>T GRCh37
NC_000009.10:g.87882772G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388711.7:c.130-446C>A ENSP00000373363.3:n.130-446C>A
ENST00000388712.7:c.130-446C>A MANE Select ENSP00000373364.3:n.130-446C>A
ENST00000466178.1:c.130-446C>A ENSP00000418155.1:n.130-446C>A
ENST00000470762.6:c.130-446C>A ENSP00000417504.2:n.130-446C>A
ENST00000472919.1:n.191-498C>A
ENST00000486130.5:c.130-446C>A ENSP00000419076.1:n.130-446C>A
NM_016548.3:c.130-446C>A NP_057632.2:n.130-446C>A
NM_177937.2:c.130-446C>A NP_808800.1:n.130-446C>A
NM_016548.4:c.130-446C>A MANE Select NP_057632.2:n.130-446C>A
NM_177937.3:c.130-446C>A NP_808800.1:n.130-446C>A