Canonical Allele Identifier: CA2245601211
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996832G= , CM000679.2:g.6996832G= GRCh38
NC_000017.10:g.6900151G= , CM000679.1:g.6900151G= GRCh37
NC_000017.9:g.6840875G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.142G= (ALOX12) MANE Select ENSP00000251535.6:p.Glu48=
ENST00000251535.10:c.142G= (ALOX12) ENSP00000251535.6:p.Glu48=
NM_000697.2:c.142G= (ALOX12) NP_000688.2:p.Glu48=
NR_040089.1:n.234-11292C= (ALOX12-AS1)
XM_011523780.1:c.499G= (ALOX12) XP_011522082.1:p.Glu167=
XM_011523780.2:c.499G= (ALOX12) XP_011522082.1:p.Glu167=
NM_000697.3:c.142G= (ALOX12) MANE Select NP_000688.2:p.Glu48=
Search 100 bp 5'
Search 100 bp 3'