Canonical Allele Identifier: CA1861294630
Gene: GOLM1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86085247T= , CM000671.2:g.86085247T= GRCh38
NC_000009.11:g.88700162T= , CM000671.1:g.88700162T= GRCh37
NC_000009.10:g.87889982T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388711.7:c.-21-5906A= ENSP00000373363.3:n.-21-5906A=
ENST00000388712.7:c.-21-5906A= MANE Select ENSP00000373364.3:n.-21-5906A=
ENST00000466178.1:c.-141-208A= ENSP00000418155.1:n.-141-208A=
ENST00000472919.1:n.150-5906A=
NM_016548.3:c.-21-5906A= NP_057632.2:n.-21-5906A=
NM_177937.2:c.-21-5906A= NP_808800.1:n.-21-5906A=
NM_016548.4:c.-21-5906A= MANE Select NP_057632.2:n.-21-5906A=
NM_177937.3:c.-21-5906A= NP_808800.1:n.-21-5906A=
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