Canonical Allele Identifier: CA1861285701
Gene: GOLM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86078368_86078369delinsGA , CM000671.2:g.86078368_86078369delinsGA GRCh38
NC_000009.11:g.88693283_88693284delinsGA , CM000671.1:g.88693283_88693284delinsGA GRCh37
NC_000009.10:g.87883103_87883104delinsGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388711.7:c.130-778_130-777delinsTC ENSP00000373363.3:n.130-778_130-777delinsTC
ENST00000388712.7:c.130-778_130-777delinsTC MANE Select ENSP00000373364.3:n.130-778_130-777delinsTC
ENST00000466178.1:c.130-778_130-777delinsTC ENSP00000418155.1:n.130-778_130-777delinsTC
ENST00000470762.6:c.130-778_130-777delinsTC ENSP00000417504.2:n.130-778_130-777delinsTC
ENST00000472919.1:n.191-830_191-829delinsTC
ENST00000486130.5:c.130-778_130-777delinsTC ENSP00000419076.1:n.130-778_130-777delinsTC
NM_016548.3:c.130-778_130-777delinsTC NP_057632.2:n.130-778_130-777delinsTC
NM_177937.2:c.130-778_130-777delinsTC NP_808800.1:n.130-778_130-777delinsTC
NM_016548.4:c.130-778_130-777delinsTC MANE Select NP_057632.2:n.130-778_130-777delinsTC
NM_177937.3:c.130-778_130-777delinsTC NP_808800.1:n.130-778_130-777delinsTC