Canonical Allele Identifier: CA2245576218
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001936_7001937delinsCA , CM000679.2:g.7001936_7001937delinsCA GRCh38
NC_000017.10:g.6905255_6905256delinsCA , CM000679.1:g.6905255_6905256delinsCA GRCh37
NC_000017.9:g.6845979_6845980delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1161+125_1161+126delinsCA (ALOX12) MANE Select ENSP00000251535.6:n.1161+125_1161+126delinsCA
ENST00000251535.10:c.1161+125_1161+126delinsCA (ALOX12) ENSP00000251535.6:n.1161+125_1161+126delinsCA
NM_000697.2:c.1161+125_1161+126delinsCA (ALOX12) NP_000688.2:n.1161+125_1161+126delinsCA
NR_040089.1:n.233+7859_233+7860delinsTG (ALOX12-AS1)
XM_011523780.1:c.1311+125_1311+126delinsCA (ALOX12) XP_011522082.1:n.1311+125_1311+126delinsCA
XM_011523780.2:c.1311+125_1311+126delinsCA (ALOX12) XP_011522082.1:n.1311+125_1311+126delinsCA
NM_000697.3:c.1161+125_1161+126delinsCA (ALOX12) MANE Select NP_000688.2:n.1161+125_1161+126delinsCA