Canonical Allele Identifier: CA2581291124
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7008372G>T , CM000679.2:g.7008372G>T GRCh38
NC_000017.10:g.6911691G>T , CM000679.1:g.6911691G>T GRCh37
NC_000017.9:g.6852415G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000251535.11:c.1541-1375G>T (ALOX12) MANE Select ENSP00000251535.6:n.1541-1375G>T
ENST00000251535.10:c.1541-1375G>T (ALOX12) ENSP00000251535.6:n.1541-1375G>T
NM_000697.2:c.1541-1375G>T (ALOX12) NP_000688.2:n.1541-1375G>T
NR_040089.1:n.233+1424C>A (ALOX12-AS1)
XM_011523780.1:c.1691-1375G>T (ALOX12) XP_011522082.1:n.1691-1375G>T
XM_011523780.2:c.1691-1375G>T (ALOX12) XP_011522082.1:n.1691-1375G>T
NM_000697.3:c.1541-1375G>T (ALOX12) MANE Select NP_000688.2:n.1541-1375G>T