Canonical Allele Identifier: CA624860189
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1567718291
gnomAD v2: 17-6905087-TC-T
gnomAD v3: 17-7001768-TC-T
gnomAD v4: 17-7001768-TC-T
MyVariant Identifiers: chr17:g.6905088del (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001769del , CM000679.2:g.7001769del GRCh38
NC_000017.10:g.6905088del , CM000679.1:g.6905088del GRCh37
NC_000017.9:g.6845812del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1119del (ALOX12) MANE Select ENSP00000251535.6:p.Ala374ProfsTer16
ENST00000251535.10:c.1119del (ALOX12) ENSP00000251535.6:p.Ala374ProfsTer16
NM_000697.2:c.1119del (ALOX12) NP_000688.2:p.Ala374ProfsTer16
NR_040089.1:n.233+8027del (ALOX12-AS1)
XM_011523780.1:c.1269del (ALOX12) XP_011522082.1:p.Ala424ProfsTer16
XM_011523780.2:c.1269del (ALOX12) XP_011522082.1:p.Ala424ProfsTer16
NM_000697.3:c.1119del (ALOX12) MANE Select NP_000688.2:p.Ala374ProfsTer16
Search 100 bp 5'
Search 100 bp 3'