Canonical Allele Identifier: CA2741515270

Gene: ALOX12 ALOX12-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7001793_7001794insGGTGGGG , CM000679.2:g.7001793_7001794insGGTGGGG	GRCh38
NC_000017.10:g.6905112_6905113insGGTGGGG , CM000679.1:g.6905112_6905113insGGTGGGG	GRCh37
NC_000017.9:g.6845836_6845837insGGTGGGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.1143_1144insGGTGGGG (ALOX12) MANE Select	ENSP00000251535.6:p.Leu382GlyfsTer?
ENST00000251535.10:c.1143_1144insGGTGGGG (ALOX12)	ENSP00000251535.6:p.Leu382GlyfsTer?
NM_000697.2:c.1143_1144insGGTGGGG (ALOX12)	NP_000688.2:p.Leu382GlyfsTer?
NR_040089.1:n.233+8002_233+8003insCCCCACC (ALOX12-AS1)
XM_011523780.1:c.1293_1294insGGTGGGG (ALOX12)	XP_011522082.1:p.Leu432GlyfsTer?
XM_011523780.2:c.1293_1294insGGTGGGG (ALOX12)	XP_011522082.1:p.Leu432GlyfsTer?
NM_000697.3:c.1143_1144insGGTGGGG (ALOX12) MANE Select	NP_000688.2:p.Leu382GlyfsTer?