Canonical Allele Identifier: CA2245600958

Gene: ALOX12 ALOX12-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6996590_6996595delinsGGGACC , CM000679.2:g.6996590_6996595delinsGGGACC	GRCh38
NC_000017.10:g.6899909_6899914delinsGGGACC , CM000679.1:g.6899909_6899914delinsGGGACC	GRCh37
NC_000017.9:g.6840633_6840638delinsGGGACC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.136-236_136-231delinsGGGACC (ALOX12) MANE Select	ENSP00000251535.6:n.136-236_136-231delinsGGGACC
ENST00000251535.10:c.136-236_136-231delinsGGGACC (ALOX12)	ENSP00000251535.6:n.136-236_136-231delinsGGGACC
NM_000697.2:c.136-236_136-231delinsGGGACC (ALOX12)	NP_000688.2:n.136-236_136-231delinsGGGACC
NR_040089.1:n.234-11055_234-11050delinsGGTCCC (ALOX12-AS1)
XM_011523780.1:c.493-236_493-231delinsGGGACC (ALOX12)	XP_011522082.1:n.493-236_493-231delinsGGGACC
XM_011523780.2:c.493-236_493-231delinsGGGACC (ALOX12)	XP_011522082.1:n.493-236_493-231delinsGGGACC
NM_000697.3:c.136-236_136-231delinsGGGACC (ALOX12) MANE Select	NP_000688.2:n.136-236_136-231delinsGGGACC