Canonical Allele Identifier: CA2508301411

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8086088_8086095del , CM000679.2:g.8086088_8086095del	GRCh38
NC_000017.10:g.7989406_7989413del , CM000679.1:g.7989406_7989413del	GRCh37
NC_000017.9:g.7930131_7930138del	NCBI36
NG_007099.1:g.6609_6616del
NG_007099.2:g.6622_6629del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.273_280del MANE Select	ENSP00000497784.1:p.Asn93TyrfsTer?
ENST00000319144.4:c.273_280del	ENSP00000315167.4:p.Asn93TyrfsTer?
NM_001139.2:c.273_280del	NP_001130.1:p.Asn93TyrfsTer?
NM_001139.3:c.273_280del MANE Select	NP_001130.1:p.Asn93TyrfsTer?