Canonical Allele Identifier: CA1861285771
Gene: GOLM1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86078439C= , CM000671.2:g.86078439C= GRCh38
NC_000009.11:g.88693354C= , CM000671.1:g.88693354C= GRCh37
NC_000009.10:g.87883174C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388711.7:c.129+753G= ENSP00000373363.3:n.129+753G=
ENST00000388712.7:c.129+753G= MANE Select ENSP00000373364.3:n.129+753G=
ENST00000466178.1:c.129+753G= ENSP00000418155.1:n.129+753G=
ENST00000470762.6:c.129+753G= ENSP00000417504.2:n.129+753G=
ENST00000472919.1:n.190+862G=
ENST00000486130.5:c.129+753G= ENSP00000419076.1:n.129+753G=
NM_016548.3:c.129+753G= NP_057632.2:n.129+753G=
NM_177937.2:c.129+753G= NP_808800.1:n.129+753G=
NM_016548.4:c.129+753G= MANE Select NP_057632.2:n.129+753G=
NM_177937.3:c.129+753G= NP_808800.1:n.129+753G=
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