Canonical Allele Identifier: CA2245576184

Gene: ALOX12 ALOX12-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7001864_7001865delinsAG , CM000679.2:g.7001864_7001865delinsAG	GRCh38
NC_000017.10:g.6905183_6905184delinsAG , CM000679.1:g.6905183_6905184delinsAG	GRCh37
NC_000017.9:g.6845907_6845908delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.1161+53_1161+54delinsAG (ALOX12) MANE Select	ENSP00000251535.6:n.1161+53_1161+54delinsAG
ENST00000251535.10:c.1161+53_1161+54delinsAG (ALOX12)	ENSP00000251535.6:n.1161+53_1161+54delinsAG
NM_000697.2:c.1161+53_1161+54delinsAG (ALOX12)	NP_000688.2:n.1161+53_1161+54delinsAG
NR_040089.1:n.233+7931_233+7932delinsCT (ALOX12-AS1)
XM_011523780.1:c.1311+53_1311+54delinsAG (ALOX12)	XP_011522082.1:n.1311+53_1311+54delinsAG
XM_011523780.2:c.1311+53_1311+54delinsAG (ALOX12)	XP_011522082.1:n.1311+53_1311+54delinsAG
NM_000697.3:c.1161+53_1161+54delinsAG (ALOX12) MANE Select	NP_000688.2:n.1161+53_1161+54delinsAG