Canonical Allele Identifier: CA981148795
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1908453606

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996660_6996661del , CM000679.2:g.6996660_6996661del GRCh38
NC_000017.10:g.6899979_6899980del , CM000679.1:g.6899979_6899980del GRCh37
NC_000017.9:g.6840703_6840704del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000251535.11:c.136-166_136-165del (ALOX12) MANE Select ENSP00000251535.6:n.136-166_136-165del
ENST00000251535.10:c.136-166_136-165del (ALOX12) ENSP00000251535.6:n.136-166_136-165del
NM_000697.2:c.136-166_136-165del (ALOX12) NP_000688.2:n.136-166_136-165del
NR_040089.1:n.234-11121_234-11120del (ALOX12-AS1)
XM_011523780.1:c.493-166_493-165del (ALOX12) XP_011522082.1:n.493-166_493-165del
XM_011523780.2:c.493-166_493-165del (ALOX12) XP_011522082.1:n.493-166_493-165del
NM_000697.3:c.136-166_136-165del (ALOX12) MANE Select NP_000688.2:n.136-166_136-165del