Canonical Allele Identifier: CA2635747816

Gene: ALOX12 ALOX12-AS1

Linked Data

• gnomAD v4: 17-7001917-AGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7001919_7001920del , CM000679.2:g.7001919_7001920del	GRCh38
NC_000017.10:g.6905238_6905239del , CM000679.1:g.6905238_6905239del	GRCh37
NC_000017.9:g.6845962_6845963del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.1161+108_1161+109del (ALOX12) MANE Select	ENSP00000251535.6:n.1161+108_1161+109del
ENST00000251535.10:c.1161+108_1161+109del (ALOX12)	ENSP00000251535.6:n.1161+108_1161+109del
NM_000697.2:c.1161+108_1161+109del (ALOX12)	NP_000688.2:n.1161+108_1161+109del
NR_040089.1:n.233+7877_233+7878del (ALOX12-AS1)
XM_011523780.1:c.1311+108_1311+109del (ALOX12)	XP_011522082.1:n.1311+108_1311+109del
XM_011523780.2:c.1311+108_1311+109del (ALOX12)	XP_011522082.1:n.1311+108_1311+109del
NM_000697.3:c.1161+108_1161+109del (ALOX12) MANE Select	NP_000688.2:n.1161+108_1161+109del