Canonical Allele Identifier: CA2245601387
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996989T= , CM000679.2:g.6996989T= GRCh38
NC_000017.10:g.6900308T= , CM000679.1:g.6900308T= GRCh37
NC_000017.9:g.6841032T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.299T= (ALOX12) MANE Select ENSP00000251535.6:p.Val100=
ENST00000251535.10:c.299T= (ALOX12) ENSP00000251535.6:p.Val100=
ENST00000480801.1:c.8T= (ALOX12) ENSP00000467033.1:p.Val3=
NM_000697.2:c.299T= (ALOX12) NP_000688.2:p.Val100=
NR_040089.1:n.234-11449A= (ALOX12-AS1)
XM_011523780.1:c.656T= (ALOX12) XP_011522082.1:p.Val219=
XM_011523780.2:c.656T= (ALOX12) XP_011522082.1:p.Val219=
NM_000697.3:c.299T= (ALOX12) MANE Select NP_000688.2:p.Val100=
Search 100 bp 5'
Search 100 bp 3'