Canonical Allele Identifier: CA2245576169

Gene: ALOX12 ALOX12-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7001824_7001826delinsCTA , CM000679.2:g.7001824_7001826delinsCTA	GRCh38
NC_000017.10:g.6905143_6905145delinsCTA , CM000679.1:g.6905143_6905145delinsCTA	GRCh37
NC_000017.9:g.6845867_6845869delinsCTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.1161+13_1161+15delinsCTA (ALOX12) MANE Select	ENSP00000251535.6:n.1161+13_1161+15delinsCTA
ENST00000251535.10:c.1161+13_1161+15delinsCTA (ALOX12)	ENSP00000251535.6:n.1161+13_1161+15delinsCTA
NM_000697.2:c.1161+13_1161+15delinsCTA (ALOX12)	NP_000688.2:n.1161+13_1161+15delinsCTA
NR_040089.1:n.233+7970_233+7972delinsTAG (ALOX12-AS1)
XM_011523780.1:c.1311+13_1311+15delinsCTA (ALOX12)	XP_011522082.1:n.1311+13_1311+15delinsCTA
XM_011523780.2:c.1311+13_1311+15delinsCTA (ALOX12)	XP_011522082.1:n.1311+13_1311+15delinsCTA
NM_000697.3:c.1161+13_1161+15delinsCTA (ALOX12) MANE Select	NP_000688.2:n.1161+13_1161+15delinsCTA