Canonical Allele Identifier: CA2246125819

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8075722_8075723delinsCA , CM000679.2:g.8075722_8075723delinsCA	GRCh38
NC_000017.10:g.7979040_7979041delinsCA , CM000679.1:g.7979040_7979041delinsCA	GRCh37
NC_000017.9:g.7919765_7919766delinsCA	NCBI36
NG_007099.1:g.16981_16982delinsTG
NG_007099.2:g.16994_16995delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1533-7_1533-6delinsTG MANE Select	ENSP00000497784.1:n.1533-7_1533-6delinsTG
ENST00000649809.1:c.597-7_597-6delinsTG	ENSP00000496845.1:n.597-7_597-6delinsTG
ENST00000319144.4:c.1533-7_1533-6delinsTG	ENSP00000315167.4:n.1533-7_1533-6delinsTG
ENST00000577351.5:n.479+452_479+453delinsTG
NM_001139.2:c.1533-7_1533-6delinsTG	NP_001130.1:n.1533-7_1533-6delinsTG
NM_001139.3:c.1533-7_1533-6delinsTG MANE Select	NP_001130.1:n.1533-7_1533-6delinsTG