Canonical Allele Identifier: CA2245601039
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996665C= , CM000679.2:g.6996665C= GRCh38
NC_000017.10:g.6899984C= , CM000679.1:g.6899984C= GRCh37
NC_000017.9:g.6840708C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000251535.11:c.136-161C= (ALOX12) MANE Select ENSP00000251535.6:n.136-161C=
ENST00000251535.10:c.136-161C= (ALOX12) ENSP00000251535.6:n.136-161C=
NM_000697.2:c.136-161C= (ALOX12) NP_000688.2:n.136-161C=
NR_040089.1:n.234-11125G= (ALOX12-AS1)
XM_011523780.1:c.493-161C= (ALOX12) XP_011522082.1:n.493-161C=
XM_011523780.2:c.493-161C= (ALOX12) XP_011522082.1:n.493-161C=
NM_000697.3:c.136-161C= (ALOX12) MANE Select NP_000688.2:n.136-161C=