Canonical Allele Identifier: CA2635747836
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v4: 17-7001956-TTTAATTAAG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001959_7001967del , CM000679.2:g.7001959_7001967del GRCh38
NC_000017.10:g.6905278_6905286del , CM000679.1:g.6905278_6905286del GRCh37
NC_000017.9:g.6846002_6846010del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1161+148_1161+156del (ALOX12) MANE Select ENSP00000251535.6:n.1161+148_1161+156del
ENST00000251535.10:c.1161+148_1161+156del (ALOX12) ENSP00000251535.6:n.1161+148_1161+156del
NM_000697.2:c.1161+148_1161+156del (ALOX12) NP_000688.2:n.1161+148_1161+156del
NR_040089.1:n.233+7831_233+7839del (ALOX12-AS1)
XM_011523780.1:c.1311+148_1311+156del (ALOX12) XP_011522082.1:n.1311+148_1311+156del
XM_011523780.2:c.1311+148_1311+156del (ALOX12) XP_011522082.1:n.1311+148_1311+156del
NM_000697.3:c.1161+148_1161+156del (ALOX12) MANE Select NP_000688.2:n.1161+148_1161+156del
Search 100 bp 5'
Search 100 bp 3'