Canonical Allele Identifier: CA588729095
Gene: GOLM1 HGNC NCBI

Linked Data

dbSNP Id: rs1284043140
gnomAD v2: 9-88699915-G-GC
gnomAD v3: 9-86085000-G-GC
gnomAD v4: 9-86085000-G-GC
MyVariant Identifiers: chr9:g.88699915_88699916insC (hg19) chr9:g.86085000_86085001insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86085001dup , CM000671.2:g.86085001dup GRCh38
NC_000009.11:g.88699916dup , CM000671.1:g.88699916dup GRCh37
NC_000009.10:g.87889736dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000388711.7:c.-21-5660dup ENSP00000373363.3:n.-21-5660dup
ENST00000388712.7:c.-21-5660dup MANE Select ENSP00000373364.3:n.-21-5660dup
ENST00000466178.1:c.-103dup ENSP00000418155.1:n.-103dup
ENST00000472919.1:n.150-5660dup
NM_016548.3:c.-21-5660dup NP_057632.2:n.-21-5660dup
NM_177937.2:c.-21-5660dup NP_808800.1:n.-21-5660dup
NM_016548.4:c.-21-5660dup MANE Select NP_057632.2:n.-21-5660dup
NM_177937.3:c.-21-5660dup NP_808800.1:n.-21-5660dup
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