Canonical Allele Identifier: CA2245601678
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6997168T= , CM000679.2:g.6997168T= GRCh38
NC_000017.10:g.6900487T= , CM000679.1:g.6900487T= GRCh37
NC_000017.9:g.6841211T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.337+141T= (ALOX12) MANE Select ENSP00000251535.6:n.337+141T=
ENST00000251535.10:c.337+141T= (ALOX12) ENSP00000251535.6:n.337+141T=
ENST00000480801.1:c.46+141T= (ALOX12) ENSP00000467033.1:n.46+141T=
NM_000697.2:c.337+141T= (ALOX12) NP_000688.2:n.337+141T=
NR_040089.1:n.234-11628A= (ALOX12-AS1)
XM_011523780.1:c.694+141T= (ALOX12) XP_011522082.1:n.694+141T=
XM_011523780.2:c.694+141T= (ALOX12) XP_011522082.1:n.694+141T=
NM_000697.3:c.337+141T= (ALOX12) MANE Select NP_000688.2:n.337+141T=
Search 100 bp 5'
Search 100 bp 3'