Canonical Allele Identifier: CA2836774512
Gene: ALOX12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075692_8075694del , CM000679.2:g.8075692_8075694del GRCh38
NC_000017.10:g.7979010_7979012del , CM000679.1:g.7979010_7979012del GRCh37
NC_000017.9:g.7919735_7919737del NCBI36
NG_007099.1:g.17015_17017del
NG_007099.2:g.17028_17030del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1560_1562del MANE Select ENSP00000497784.1:p.Tyr521del
ENST00000649809.1:c.624_626del ENSP00000496845.1:p.Tyr209del
ENST00000319144.4:c.1560_1562del ENSP00000315167.4:p.Tyr521del
ENST00000577351.5:n.479+486_479+488del
NM_001139.2:c.1560_1562del NP_001130.1:p.Tyr521del
NM_001139.3:c.1560_1562del MANE Select NP_001130.1:p.Tyr521del