Canonical Allele Identifier: CA2838748007

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8076432del , CM000679.2:g.8076432del	GRCh38
NC_000017.10:g.7979750del , CM000679.1:g.7979750del	GRCh37
NC_000017.9:g.7920475del	NCBI36
NG_007099.1:g.16273del
NG_007099.2:g.16286del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1363-87del MANE Select	ENSP00000497784.1:n.1363-87del
ENST00000649809.1:c.427-87del	ENSP00000496845.1:n.427-87del
ENST00000319144.4:c.1363-87del	ENSP00000315167.4:n.1363-87del
ENST00000577351.5:n.310-87del
ENST00000583276.5:n.747-87del
ENST00000584116.1:n.619-87del
NM_001139.2:c.1363-87del	NP_001130.1:n.1363-87del
NM_001139.3:c.1363-87del MANE Select	NP_001130.1:n.1363-87del