Canonical Allele Identifier: CA2832570356

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8075791dup , CM000679.2:g.8075791dup	GRCh38
NC_000017.10:g.7979109dup , CM000679.1:g.7979109dup	GRCh37
NC_000017.9:g.7919834dup	NCBI36
NG_007099.1:g.16917dup
NG_007099.2:g.16930dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1533-71dup MANE Select	ENSP00000497784.1:n.1533-71dup
ENST00000649809.1:c.597-71dup	ENSP00000496845.1:n.597-71dup
ENST00000319144.4:c.1533-71dup	ENSP00000315167.4:n.1533-71dup
ENST00000577351.5:n.479+388dup
NM_001139.2:c.1533-71dup	NP_001130.1:n.1533-71dup
NM_001139.3:c.1533-71dup MANE Select	NP_001130.1:n.1533-71dup