Canonical Allele Identifier: CA2576161240

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8086226_8086228del , CM000679.2:g.8086226_8086228del	GRCh38
NC_000017.10:g.7989544_7989546del , CM000679.1:g.7989544_7989546del	GRCh37
NC_000017.9:g.7930269_7930271del	NCBI36
NG_007099.1:g.6477_6479del
NG_007099.2:g.6490_6492del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.148-7_148-5del MANE Select	ENSP00000497784.1:n.148-7_148-5del
ENST00000319144.4:c.148-7_148-5del	ENSP00000315167.4:n.148-7_148-5del
NM_001139.2:c.148-7_148-5del	NP_001130.1:n.148-7_148-5del
NM_001139.3:c.148-7_148-5del MANE Select	NP_001130.1:n.148-7_148-5del