Canonical Allele Identifier: CA2635746111

Gene: ALOX12 ALOX12-AS1

Linked Data

• gnomAD v4: 17-6996985-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6996988del , CM000679.2:g.6996988del	GRCh38
NC_000017.10:g.6900307del , CM000679.1:g.6900307del	GRCh37
NC_000017.9:g.6841031del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.298del (ALOX12) MANE Select	ENSP00000251535.6:p.Val100CysfsTer7
ENST00000251535.10:c.298del (ALOX12)	ENSP00000251535.6:p.Val100CysfsTer7
ENST00000480801.1:c.7del (ALOX12)	ENSP00000467033.1:p.Val3CysfsTer7
NM_000697.2:c.298del (ALOX12)	NP_000688.2:p.Val100CysfsTer7
NR_040089.1:n.234-11446del (ALOX12-AS1)
XM_011523780.1:c.655del (ALOX12)	XP_011522082.1:p.Val219CysfsTer7
XM_011523780.2:c.655del (ALOX12)	XP_011522082.1:p.Val219CysfsTer7
NM_000697.3:c.298del (ALOX12) MANE Select	NP_000688.2:p.Val100CysfsTer7