Canonical Allele Identifier: CA397748763
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001752G>A , CM000679.2:g.7001752G>A GRCh38
NC_000017.10:g.6905071G>A , CM000679.1:g.6905071G>A GRCh37
NC_000017.9:g.6845795G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1102G>A (ALOX12) MANE Select ENSP00000251535.6:p.Ala368Thr
ENST00000251535.10:c.1102G>A (ALOX12) ENSP00000251535.6:p.Ala368Thr
NM_000697.2:c.1102G>A (ALOX12) NP_000688.2:p.Ala368Thr
NR_040089.1:n.233+8044C>T (ALOX12-AS1)
XM_011523780.1:c.1252G>A (ALOX12) XP_011522082.1:p.Ala418Thr
XM_011523780.2:c.1252G>A (ALOX12) XP_011522082.1:p.Ala418Thr
NM_000697.3:c.1102G>A (ALOX12) MANE Select NP_000688.2:p.Ala368Thr