Canonical Allele Identifier: CA2542069403

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8086096_8086097insAC , CM000679.2:g.8086096_8086097insAC	GRCh38
NC_000017.10:g.7989414_7989415insAC , CM000679.1:g.7989414_7989415insAC	GRCh37
NC_000017.9:g.7930139_7930140insAC	NCBI36
NG_007099.1:g.6607_6608insGT
NG_007099.2:g.6620_6621insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.271_272insGT MANE Select	ENSP00000497784.1:p.Ala91GlyfsTer?
ENST00000319144.4:c.271_272insGT	ENSP00000315167.4:p.Ala91GlyfsTer?
NM_001139.2:c.271_272insGT	NP_001130.1:p.Ala91GlyfsTer?
NM_001139.3:c.271_272insGT MANE Select	NP_001130.1:p.Ala91GlyfsTer?