Canonical Allele Identifier: CA2576145316

Gene: ALOX12 ALOX12-AS1

Linked Data

• gnomAD v4: 17-7001515-TCTTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7001520_7001523del , CM000679.2:g.7001520_7001523del	GRCh38
NC_000017.10:g.6904839_6904842del , CM000679.1:g.6904839_6904842del	GRCh37
NC_000017.9:g.6845563_6845566del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.952-82_952-79del (ALOX12) MANE Select	ENSP00000251535.6:n.952-82_952-79del
ENST00000251535.10:c.952-82_952-79del (ALOX12)	ENSP00000251535.6:n.952-82_952-79del
NM_000697.2:c.952-82_952-79del (ALOX12)	NP_000688.2:n.952-82_952-79del
NR_040089.1:n.233+8277_233+8280del (ALOX12-AS1)
XM_011523780.1:c.1102-82_1102-79del (ALOX12)	XP_011522082.1:n.1102-82_1102-79del
XM_011523780.2:c.1102-82_1102-79del (ALOX12)	XP_011522082.1:n.1102-82_1102-79del
NM_000697.3:c.952-82_952-79del (ALOX12) MANE Select	NP_000688.2:n.952-82_952-79del