Canonical Allele Identifier: CA1861285391
Gene: GOLM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86078050_86078051delinsAG , CM000671.2:g.86078050_86078051delinsAG GRCh38
NC_000009.11:g.88692965_88692966delinsAG , CM000671.1:g.88692965_88692966delinsAG GRCh37
NC_000009.10:g.87882785_87882786delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388711.7:c.130-460_130-459delinsCT ENSP00000373363.3:n.130-460_130-459delinsCT
ENST00000388712.7:c.130-460_130-459delinsCT MANE Select ENSP00000373364.3:n.130-460_130-459delinsCT
ENST00000466178.1:c.130-460_130-459delinsCT ENSP00000418155.1:n.130-460_130-459delinsCT
ENST00000470762.6:c.130-460_130-459delinsCT ENSP00000417504.2:n.130-460_130-459delinsCT
ENST00000472919.1:n.191-512_191-511delinsCT
ENST00000486130.5:c.130-460_130-459delinsCT ENSP00000419076.1:n.130-460_130-459delinsCT
NM_016548.3:c.130-460_130-459delinsCT NP_057632.2:n.130-460_130-459delinsCT
NM_177937.2:c.130-460_130-459delinsCT NP_808800.1:n.130-460_130-459delinsCT
NM_016548.4:c.130-460_130-459delinsCT MANE Select NP_057632.2:n.130-460_130-459delinsCT
NM_177937.3:c.130-460_130-459delinsCT NP_808800.1:n.130-460_130-459delinsCT