Canonical Allele Identifier: CA2690505029
Gene: GOLM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86084961_86084962del , CM000671.2:g.86084961_86084962del GRCh38
NC_000009.11:g.88699876_88699877del , CM000671.1:g.88699876_88699877del GRCh37
NC_000009.10:g.87889696_87889697del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000388711.7:c.-21-5621_-21-5620del ENSP00000373363.3:n.-21-5621_-21-5620del
ENST00000388712.7:c.-21-5621_-21-5620del MANE Select ENSP00000373364.3:n.-21-5621_-21-5620del
ENST00000466178.1:c.-64_-63del ENSP00000418155.1:n.-64_-63del
ENST00000472919.1:n.150-5621_150-5620del
NM_016548.3:c.-21-5621_-21-5620del NP_057632.2:n.-21-5621_-21-5620del
NM_177937.2:c.-21-5621_-21-5620del NP_808800.1:n.-21-5621_-21-5620del
NM_016548.4:c.-21-5621_-21-5620del MANE Select NP_057632.2:n.-21-5621_-21-5620del
NM_177937.3:c.-21-5621_-21-5620del NP_808800.1:n.-21-5621_-21-5620del