Canonical Allele Identifier: CA2808396420

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8086293_8086294insAA , CM000679.2:g.8086293_8086294insAA	GRCh38
NC_000017.10:g.7989611_7989612insAA , CM000679.1:g.7989611_7989612insAA	GRCh37
NC_000017.9:g.7930336_7930337insAA	NCBI36
NG_007099.1:g.6410_6411insTT
NG_007099.2:g.6423_6424insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.148-74_148-73insTT MANE Select	ENSP00000497784.1:n.148-74_148-73insTT
ENST00000319144.4:c.148-74_148-73insTT	ENSP00000315167.4:n.148-74_148-73insTT
NM_001139.2:c.148-74_148-73insTT	NP_001130.1:n.148-74_148-73insTT
NM_001139.3:c.148-74_148-73insTT MANE Select	NP_001130.1:n.148-74_148-73insTT