Canonical Allele Identifier: CA2245601493
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6997041_6997042delinsGT , CM000679.2:g.6997041_6997042delinsGT GRCh38
NC_000017.10:g.6900360_6900361delinsGT , CM000679.1:g.6900360_6900361delinsGT GRCh37
NC_000017.9:g.6841084_6841085delinsGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.337+14_337+15delinsGT (ALOX12) MANE Select ENSP00000251535.6:n.337+14_337+15delinsGT
ENST00000251535.10:c.337+14_337+15delinsGT (ALOX12) ENSP00000251535.6:n.337+14_337+15delinsGT
ENST00000480801.1:c.46+14_46+15delinsGT (ALOX12) ENSP00000467033.1:n.46+14_46+15delinsGT
NM_000697.2:c.337+14_337+15delinsGT (ALOX12) NP_000688.2:n.337+14_337+15delinsGT
NR_040089.1:n.234-11502_234-11501delinsAC (ALOX12-AS1)
XM_011523780.1:c.694+14_694+15delinsGT (ALOX12) XP_011522082.1:n.694+14_694+15delinsGT
XM_011523780.2:c.694+14_694+15delinsGT (ALOX12) XP_011522082.1:n.694+14_694+15delinsGT
NM_000697.3:c.337+14_337+15delinsGT (ALOX12) MANE Select NP_000688.2:n.337+14_337+15delinsGT
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