Canonical Allele Identifier: CA2245601473

Gene: ALOX12 ALOX12-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6997034_6997037delinsAGGC , CM000679.2:g.6997034_6997037delinsAGGC	GRCh38
NC_000017.10:g.6900353_6900356delinsAGGC , CM000679.1:g.6900353_6900356delinsAGGC	GRCh37
NC_000017.9:g.6841077_6841080delinsAGGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.337+7_337+10delinsAGGC (ALOX12) MANE Select	ENSP00000251535.6:n.337+7_337+10delinsAGGC
ENST00000251535.10:c.337+7_337+10delinsAGGC (ALOX12)	ENSP00000251535.6:n.337+7_337+10delinsAGGC
ENST00000480801.1:c.46+7_46+10delinsAGGC (ALOX12)	ENSP00000467033.1:n.46+7_46+10delinsAGGC
NM_000697.2:c.337+7_337+10delinsAGGC (ALOX12)	NP_000688.2:n.337+7_337+10delinsAGGC
NR_040089.1:n.234-11497_234-11494delinsGCCT (ALOX12-AS1)
XM_011523780.1:c.694+7_694+10delinsAGGC (ALOX12)	XP_011522082.1:n.694+7_694+10delinsAGGC
XM_011523780.2:c.694+7_694+10delinsAGGC (ALOX12)	XP_011522082.1:n.694+7_694+10delinsAGGC
NM_000697.3:c.337+7_337+10delinsAGGC (ALOX12) MANE Select	NP_000688.2:n.337+7_337+10delinsAGGC