Canonical Allele Identifier: CA2245601095

Gene: ALOX12 ALOX12-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6996728_6996730delinsCCT , CM000679.2:g.6996728_6996730delinsCCT	GRCh38
NC_000017.10:g.6900047_6900049delinsCCT , CM000679.1:g.6900047_6900049delinsCCT	GRCh37
NC_000017.9:g.6840771_6840773delinsCCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.136-98_136-96delinsCCT (ALOX12) MANE Select	ENSP00000251535.6:n.136-98_136-96delinsCCT
ENST00000251535.10:c.136-98_136-96delinsCCT (ALOX12)	ENSP00000251535.6:n.136-98_136-96delinsCCT
NM_000697.2:c.136-98_136-96delinsCCT (ALOX12)	NP_000688.2:n.136-98_136-96delinsCCT
NR_040089.1:n.234-11190_234-11188delinsAGG (ALOX12-AS1)
XM_011523780.1:c.493-98_493-96delinsCCT (ALOX12)	XP_011522082.1:n.493-98_493-96delinsCCT
XM_011523780.2:c.493-98_493-96delinsCCT (ALOX12)	XP_011522082.1:n.493-98_493-96delinsCCT
NM_000697.3:c.136-98_136-96delinsCCT (ALOX12) MANE Select	NP_000688.2:n.136-98_136-96delinsCCT