Canonical Allele Identifier: CA2576145168
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996735A>C , CM000679.2:g.6996735A>C GRCh38
NC_000017.10:g.6900054A>C , CM000679.1:g.6900054A>C GRCh37
NC_000017.9:g.6840778A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.136-91A>C (ALOX12) MANE Select ENSP00000251535.6:n.136-91A>C
ENST00000251535.10:c.136-91A>C (ALOX12) ENSP00000251535.6:n.136-91A>C
NM_000697.2:c.136-91A>C (ALOX12) NP_000688.2:n.136-91A>C
NR_040089.1:n.234-11195T>G (ALOX12-AS1)
XM_011523780.1:c.493-91A>C (ALOX12) XP_011522082.1:n.493-91A>C
XM_011523780.2:c.493-91A>C (ALOX12) XP_011522082.1:n.493-91A>C
NM_000697.3:c.136-91A>C (ALOX12) MANE Select NP_000688.2:n.136-91A>C