Canonical Allele Identifier: CA867920600
Gene: GOLM1 HGNC NCBI

Linked Data

dbSNP Id: rs1201121820
MyVariant Identifiers: chr9:g.88700025del (hg19) chr9:g.86085110del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86085113del , CM000671.2:g.86085113del GRCh38
NC_000009.11:g.88700028del , CM000671.1:g.88700028del GRCh37
NC_000009.10:g.87889848del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000388711.7:c.-21-5769del ENSP00000373363.3:n.-21-5769del
ENST00000388712.7:c.-21-5769del MANE Select ENSP00000373364.3:n.-21-5769del
ENST00000466178.1:c.-141-71del ENSP00000418155.1:n.-141-71del
ENST00000472919.1:n.150-5769del
NM_016548.3:c.-21-5769del NP_057632.2:n.-21-5769del
NM_177937.2:c.-21-5769del NP_808800.1:n.-21-5769del
NM_016548.4:c.-21-5769del MANE Select NP_057632.2:n.-21-5769del
NM_177937.3:c.-21-5769del NP_808800.1:n.-21-5769del
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