Canonical Allele Identifier: CA2635746003

Gene: ALOX12 ALOX12-AS1

Linked Data

• gnomAD v4: 17-6996700-G-GGAACGA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6996702_6996707dup , CM000679.2:g.6996702_6996707dup	GRCh38
NC_000017.10:g.6900021_6900026dup , CM000679.1:g.6900021_6900026dup	GRCh37
NC_000017.9:g.6840745_6840750dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.136-124_136-119dup (ALOX12) MANE Select	ENSP00000251535.6:n.136-124_136-119dup
ENST00000251535.10:c.136-124_136-119dup (ALOX12)	ENSP00000251535.6:n.136-124_136-119dup
NM_000697.2:c.136-124_136-119dup (ALOX12)	NP_000688.2:n.136-124_136-119dup
NR_040089.1:n.234-11166_234-11161dup (ALOX12-AS1)
XM_011523780.1:c.493-124_493-119dup (ALOX12)	XP_011522082.1:n.493-124_493-119dup
XM_011523780.2:c.493-124_493-119dup (ALOX12)	XP_011522082.1:n.493-124_493-119dup
NM_000697.3:c.136-124_136-119dup (ALOX12) MANE Select	NP_000688.2:n.136-124_136-119dup