Canonical Allele Identifier: CA2635747734
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v4: 17-7001509-C-CAAT
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001513_7001515dup , CM000679.2:g.7001513_7001515dup GRCh38
NC_000017.10:g.6904832_6904834dup , CM000679.1:g.6904832_6904834dup GRCh37
NC_000017.9:g.6845556_6845558dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.952-89_952-87dup (ALOX12) MANE Select ENSP00000251535.6:n.952-89_952-87dup
ENST00000251535.10:c.952-89_952-87dup (ALOX12) ENSP00000251535.6:n.952-89_952-87dup
NM_000697.2:c.952-89_952-87dup (ALOX12) NP_000688.2:n.952-89_952-87dup
NR_040089.1:n.233+8284_233+8286dup (ALOX12-AS1)
XM_011523780.1:c.1102-89_1102-87dup (ALOX12) XP_011522082.1:n.1102-89_1102-87dup
XM_011523780.2:c.1102-89_1102-87dup (ALOX12) XP_011522082.1:n.1102-89_1102-87dup
NM_000697.3:c.952-89_952-87dup (ALOX12) MANE Select NP_000688.2:n.952-89_952-87dup
Search 100 bp 5'
Search 100 bp 3'