Canonical Allele Identifier: CA2246126668

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8076544_8076545delinsCT , CM000679.2:g.8076544_8076545delinsCT	GRCh38
NC_000017.10:g.7979862_7979863delinsCT , CM000679.1:g.7979862_7979863delinsCT	GRCh37
NC_000017.9:g.7920587_7920588delinsCT	NCBI36
NG_007099.1:g.16159_16160delinsAG
NG_007099.2:g.16172_16173delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1362+112_1362+113delinsAG MANE Select	ENSP00000497784.1:n.1362+112_1362+113delinsAG
ENST00000649809.1:c.426+112_426+113delinsAG	ENSP00000496845.1:n.426+112_426+113delinsAG
ENST00000319144.4:c.1362+112_1362+113delinsAG	ENSP00000315167.4:n.1362+112_1362+113delinsAG
ENST00000577351.5:n.309+112_309+113delinsAG
ENST00000583276.5:n.746+112_746+113delinsAG
ENST00000584116.1:n.618+112_618+113delinsAG
NM_001139.2:c.1362+112_1362+113delinsAG	NP_001130.1:n.1362+112_1362+113delinsAG
NM_001139.3:c.1362+112_1362+113delinsAG MANE Select	NP_001130.1:n.1362+112_1362+113delinsAG