Canonical Allele Identifier: CA1861285594
Gene: GOLM1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86078269A= , CM000671.2:g.86078269A= GRCh38
NC_000009.11:g.88693184A= , CM000671.1:g.88693184A= GRCh37
NC_000009.10:g.87883004A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388711.7:c.130-678T= ENSP00000373363.3:n.130-678T=
ENST00000388712.7:c.130-678T= MANE Select ENSP00000373364.3:n.130-678T=
ENST00000466178.1:c.130-678T= ENSP00000418155.1:n.130-678T=
ENST00000470762.6:c.130-678T= ENSP00000417504.2:n.130-678T=
ENST00000472919.1:n.191-730T=
ENST00000486130.5:c.130-678T= ENSP00000419076.1:n.130-678T=
NM_016548.3:c.130-678T= NP_057632.2:n.130-678T=
NM_177937.2:c.130-678T= NP_808800.1:n.130-678T=
NM_016548.4:c.130-678T= MANE Select NP_057632.2:n.130-678T=
NM_177937.3:c.130-678T= NP_808800.1:n.130-678T=
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