Canonical Allele Identifier: CA2590132277
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v3: 17-7001988-CATT-C
gnomAD v4: 17-7001988-CATT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001991_7001993del , CM000679.2:g.7001991_7001993del GRCh38
NC_000017.10:g.6905310_6905312del , CM000679.1:g.6905310_6905312del GRCh37
NC_000017.9:g.6846034_6846036del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1161+180_1161+182del (ALOX12) MANE Select ENSP00000251535.6:n.1161+180_1161+182del
ENST00000251535.10:c.1161+180_1161+182del (ALOX12) ENSP00000251535.6:n.1161+180_1161+182del
NM_000697.2:c.1161+180_1161+182del (ALOX12) NP_000688.2:n.1161+180_1161+182del
NR_040089.1:n.233+7805_233+7807del (ALOX12-AS1)
XM_011523780.1:c.1311+180_1311+182del (ALOX12) XP_011522082.1:n.1311+180_1311+182del
XM_011523780.2:c.1311+180_1311+182del (ALOX12) XP_011522082.1:n.1311+180_1311+182del
NM_000697.3:c.1161+180_1161+182del (ALOX12) MANE Select NP_000688.2:n.1161+180_1161+182del
Search 100 bp 5'
Search 100 bp 3'