Canonical Allele Identifier: CA2635747779
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v4: 17-7001851-CAGAG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001856_7001859del , CM000679.2:g.7001856_7001859del GRCh38
NC_000017.10:g.6905175_6905178del , CM000679.1:g.6905175_6905178del GRCh37
NC_000017.9:g.6845899_6845902del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1161+45_1161+48del (ALOX12) MANE Select ENSP00000251535.6:n.1161+45_1161+48del
ENST00000251535.10:c.1161+45_1161+48del (ALOX12) ENSP00000251535.6:n.1161+45_1161+48del
NM_000697.2:c.1161+45_1161+48del (ALOX12) NP_000688.2:n.1161+45_1161+48del
NR_040089.1:n.233+7941_233+7944del (ALOX12-AS1)
XM_011523780.1:c.1311+45_1311+48del (ALOX12) XP_011522082.1:n.1311+45_1311+48del
XM_011523780.2:c.1311+45_1311+48del (ALOX12) XP_011522082.1:n.1311+45_1311+48del
NM_000697.3:c.1161+45_1161+48del (ALOX12) MANE Select NP_000688.2:n.1161+45_1161+48del
Search 100 bp 5'
Search 100 bp 3'