Canonical Allele Identifier: CA867916218

Gene: GOLM1

Linked Data

• dbSNP Id: rs1386235323
• gnomAD v3: 9-86078537-TG-T
• gnomAD v4: 9-86078537-TG-T
• MyVariant Identifiers: chr9:g.88693453del (hg19) ; chr9:g.86078538del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.86078539del , CM000671.2:g.86078539del	GRCh38
NC_000009.11:g.88693454del , CM000671.1:g.88693454del	GRCh37
NC_000009.10:g.87883274del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388711.7:c.129+654del	ENSP00000373363.3:n.129+654del
ENST00000388712.7:c.129+654del MANE Select	ENSP00000373364.3:n.129+654del
ENST00000466178.1:c.129+654del	ENSP00000418155.1:n.129+654del
ENST00000470762.6:c.129+654del	ENSP00000417504.2:n.129+654del
ENST00000472919.1:n.190+763del
ENST00000486130.5:c.129+654del	ENSP00000419076.1:n.129+654del
NM_016548.3:c.129+654del	NP_057632.2:n.129+654del
NM_177937.2:c.129+654del	NP_808800.1:n.129+654del
NM_016548.4:c.129+654del MANE Select	NP_057632.2:n.129+654del
NM_177937.3:c.129+654del	NP_808800.1:n.129+654del