Canonical Allele Identifier: CA2245601007
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996634T= , CM000679.2:g.6996634T= GRCh38
NC_000017.10:g.6899953T= , CM000679.1:g.6899953T= GRCh37
NC_000017.9:g.6840677T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.136-192T= (ALOX12) MANE Select ENSP00000251535.6:n.136-192T=
ENST00000251535.10:c.136-192T= (ALOX12) ENSP00000251535.6:n.136-192T=
NM_000697.2:c.136-192T= (ALOX12) NP_000688.2:n.136-192T=
NR_040089.1:n.234-11094A= (ALOX12-AS1)
XM_011523780.1:c.493-192T= (ALOX12) XP_011522082.1:n.493-192T=
XM_011523780.2:c.493-192T= (ALOX12) XP_011522082.1:n.493-192T=
NM_000697.3:c.136-192T= (ALOX12) MANE Select NP_000688.2:n.136-192T=
Search 100 bp 5'
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