Canonical Allele Identifier: CA2245576202
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001912T= , CM000679.2:g.7001912T= GRCh38
NC_000017.10:g.6905231T= , CM000679.1:g.6905231T= GRCh37
NC_000017.9:g.6845955T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1161+101T= (ALOX12) MANE Select ENSP00000251535.6:n.1161+101T=
ENST00000251535.10:c.1161+101T= (ALOX12) ENSP00000251535.6:n.1161+101T=
NM_000697.2:c.1161+101T= (ALOX12) NP_000688.2:n.1161+101T=
NR_040089.1:n.233+7884A= (ALOX12-AS1)
XM_011523780.1:c.1311+101T= (ALOX12) XP_011522082.1:n.1311+101T=
XM_011523780.2:c.1311+101T= (ALOX12) XP_011522082.1:n.1311+101T=
NM_000697.3:c.1161+101T= (ALOX12) MANE Select NP_000688.2:n.1161+101T=
Search 100 bp 5'
Search 100 bp 3'