Canonical Allele Identifier: CA2832570354

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8075567dup , CM000679.2:g.8075567dup	GRCh38
NC_000017.10:g.7978885dup , CM000679.1:g.7978885dup	GRCh37
NC_000017.9:g.7919610dup	NCBI36
NG_007099.1:g.17141dup
NG_007099.2:g.17154dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1654+32dup MANE Select	ENSP00000497784.1:n.1654+32dup
ENST00000649809.1:c.718+32dup	ENSP00000496845.1:n.718+32dup
ENST00000319144.4:c.1654+32dup	ENSP00000315167.4:n.1654+32dup
ENST00000577351.5:n.479+612dup
NM_001139.2:c.1654+32dup	NP_001130.1:n.1654+32dup
NM_001139.3:c.1654+32dup MANE Select	NP_001130.1:n.1654+32dup