Canonical Allele Identifier: CA2246126611

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8076488_8076489delinsCA , CM000679.2:g.8076488_8076489delinsCA	GRCh38
NC_000017.10:g.7979806_7979807delinsCA , CM000679.1:g.7979806_7979807delinsCA	GRCh37
NC_000017.9:g.7920531_7920532delinsCA	NCBI36
NG_007099.1:g.16215_16216delinsTG
NG_007099.2:g.16228_16229delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1363-145_1363-144delinsTG MANE Select	ENSP00000497784.1:n.1363-145_1363-144delinsTG
ENST00000649809.1:c.427-145_427-144delinsTG	ENSP00000496845.1:n.427-145_427-144delinsTG
ENST00000319144.4:c.1363-145_1363-144delinsTG	ENSP00000315167.4:n.1363-145_1363-144delinsTG
ENST00000577351.5:n.310-145_310-144delinsTG
ENST00000583276.5:n.747-145_747-144delinsTG
ENST00000584116.1:n.619-145_619-144delinsTG
NM_001139.2:c.1363-145_1363-144delinsTG	NP_001130.1:n.1363-145_1363-144delinsTG
NM_001139.3:c.1363-145_1363-144delinsTG MANE Select	NP_001130.1:n.1363-145_1363-144delinsTG