Canonical Allele Identifier: CA2245577818
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7004939T= , CM000679.2:g.7004939T= GRCh38
NC_000017.10:g.6908258T= , CM000679.1:g.6908258T= GRCh37
NC_000017.9:g.6848982T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000251535.11:c.1162-318T= (ALOX12) MANE Select ENSP00000251535.6:n.1162-318T=
ENST00000251535.10:c.1162-318T= (ALOX12) ENSP00000251535.6:n.1162-318T=
NM_000697.2:c.1162-318T= (ALOX12) NP_000688.2:n.1162-318T=
NR_040089.1:n.233+4857A= (ALOX12-AS1)
XM_011523780.1:c.1312-318T= (ALOX12) XP_011522082.1:n.1312-318T=
XM_011523780.2:c.1312-318T= (ALOX12) XP_011522082.1:n.1312-318T=
NM_000697.3:c.1162-318T= (ALOX12) MANE Select NP_000688.2:n.1162-318T=
Search 100 bp 5'
Search 100 bp 3'