Canonical Allele Identifier: CA2808360543

Gene: ALOX12 ALOX12-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7001970_7001978dup , CM000679.2:g.7001970_7001978dup	GRCh38
NC_000017.10:g.6905289_6905297dup , CM000679.1:g.6905289_6905297dup	GRCh37
NC_000017.9:g.6846013_6846021dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.1161+159_1161+167dup (ALOX12) MANE Select	ENSP00000251535.6:n.1161+159_1161+167dup
ENST00000251535.10:c.1161+159_1161+167dup (ALOX12)	ENSP00000251535.6:n.1161+159_1161+167dup
NM_000697.2:c.1161+159_1161+167dup (ALOX12)	NP_000688.2:n.1161+159_1161+167dup
NR_040089.1:n.233+7828_233+7836dup (ALOX12-AS1)
XM_011523780.1:c.1311+159_1311+167dup (ALOX12)	XP_011522082.1:n.1311+159_1311+167dup
XM_011523780.2:c.1311+159_1311+167dup (ALOX12)	XP_011522082.1:n.1311+159_1311+167dup
NM_000697.3:c.1161+159_1161+167dup (ALOX12) MANE Select	NP_000688.2:n.1161+159_1161+167dup