Canonical Allele Identifier: CA397737898
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v4: 17-6996958-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996958G>A , CM000679.2:g.6996958G>A GRCh38
NC_000017.10:g.6900277G>A , CM000679.1:g.6900277G>A GRCh37
NC_000017.9:g.6841001G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.268G>A (ALOX12) MANE Select ENSP00000251535.6:p.Ala90Thr
ENST00000251535.10:c.268G>A (ALOX12) ENSP00000251535.6:p.Ala90Thr
NM_000697.2:c.268G>A (ALOX12) NP_000688.2:p.Ala90Thr
NR_040089.1:n.234-11418C>T (ALOX12-AS1)
XM_011523780.1:c.625G>A (ALOX12) XP_011522082.1:p.Ala209Thr
XM_011523780.2:c.625G>A (ALOX12) XP_011522082.1:p.Ala209Thr
NM_000697.3:c.268G>A (ALOX12) MANE Select NP_000688.2:p.Ala90Thr