Canonical Allele Identifier: CA2635747760

Gene: ALOX12 ALOX12-AS1

Linked Data

• gnomAD v4: 17-7001715-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7001715_7001716insA , CM000679.2:g.7001715_7001716insA	GRCh38
NC_000017.10:g.6905034_6905035insA , CM000679.1:g.6905034_6905035insA	GRCh37
NC_000017.9:g.6845758_6845759insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.1065_1066insA (ALOX12) MANE Select	ENSP00000251535.6:p.Glu356ArgfsTer14
ENST00000251535.10:c.1065_1066insA (ALOX12)	ENSP00000251535.6:p.Glu356ArgfsTer14
NM_000697.2:c.1065_1066insA (ALOX12)	NP_000688.2:p.Glu356ArgfsTer14
NR_040089.1:n.233+8080_233+8081insT (ALOX12-AS1)
XM_011523780.1:c.1215_1216insA (ALOX12)	XP_011522082.1:p.Glu406ArgfsTer14
XM_011523780.2:c.1215_1216insA (ALOX12)	XP_011522082.1:p.Glu406ArgfsTer14
NM_000697.3:c.1065_1066insA (ALOX12) MANE Select	NP_000688.2:p.Glu356ArgfsTer14