Canonical Allele Identifier: CA2245576240
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001988C= , CM000679.2:g.7001988C= GRCh38
NC_000017.10:g.6905307C= , CM000679.1:g.6905307C= GRCh37
NC_000017.9:g.6846031C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1161+177C= (ALOX12) MANE Select ENSP00000251535.6:n.1161+177C=
ENST00000251535.10:c.1161+177C= (ALOX12) ENSP00000251535.6:n.1161+177C=
NM_000697.2:c.1161+177C= (ALOX12) NP_000688.2:n.1161+177C=
NR_040089.1:n.233+7808G= (ALOX12-AS1)
XM_011523780.1:c.1311+177C= (ALOX12) XP_011522082.1:n.1311+177C=
XM_011523780.2:c.1311+177C= (ALOX12) XP_011522082.1:n.1311+177C=
NM_000697.3:c.1161+177C= (ALOX12) MANE Select NP_000688.2:n.1161+177C=
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