Canonical Allele Identifier: CA1861294550
Gene: GOLM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86085069T= , CM000671.2:g.86085069T= GRCh38
NC_000009.11:g.88699984T= , CM000671.1:g.88699984T= GRCh37
NC_000009.10:g.87889804T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000388711.7:c.-21-5728A= ENSP00000373363.3:n.-21-5728A=
ENST00000388712.7:c.-21-5728A= MANE Select ENSP00000373364.3:n.-21-5728A=
ENST00000466178.1:c.-141-30A= ENSP00000418155.1:n.-141-30A=
ENST00000472919.1:n.150-5728A=
NM_016548.3:c.-21-5728A= NP_057632.2:n.-21-5728A=
NM_177937.2:c.-21-5728A= NP_808800.1:n.-21-5728A=
NM_016548.4:c.-21-5728A= MANE Select NP_057632.2:n.-21-5728A=
NM_177937.3:c.-21-5728A= NP_808800.1:n.-21-5728A=