Canonical Allele Identifier: CA2245576175

Gene: ALOX12 ALOX12-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7001847_7001849delinsACC , CM000679.2:g.7001847_7001849delinsACC	GRCh38
NC_000017.10:g.6905166_6905168delinsACC , CM000679.1:g.6905166_6905168delinsACC	GRCh37
NC_000017.9:g.6845890_6845892delinsACC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.1161+36_1161+38delinsACC (ALOX12) MANE Select	ENSP00000251535.6:n.1161+36_1161+38delinsACC
ENST00000251535.10:c.1161+36_1161+38delinsACC (ALOX12)	ENSP00000251535.6:n.1161+36_1161+38delinsACC
NM_000697.2:c.1161+36_1161+38delinsACC (ALOX12)	NP_000688.2:n.1161+36_1161+38delinsACC
NR_040089.1:n.233+7947_233+7949delinsGGT (ALOX12-AS1)
XM_011523780.1:c.1311+36_1311+38delinsACC (ALOX12)	XP_011522082.1:n.1311+36_1311+38delinsACC
XM_011523780.2:c.1311+36_1311+38delinsACC (ALOX12)	XP_011522082.1:n.1311+36_1311+38delinsACC
NM_000697.3:c.1161+36_1161+38delinsACC (ALOX12) MANE Select	NP_000688.2:n.1161+36_1161+38delinsACC