Canonical Allele Identifier: CA2741515272

Gene: ALOX12 ALOX12-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7001796_7001797insAAAGAAGAGAACTATGGCATA , CM000679.2:g.7001796_7001797insAAAGAAGAGAACTATGGCATA	GRCh38
NC_000017.10:g.6905115_6905116insAAAGAAGAGAACTATGGCATA , CM000679.1:g.6905115_6905116insAAAGAAGAGAACTATGGCATA	GRCh37
NC_000017.9:g.6845839_6845840insAAAGAAGAGAACTATGGCATA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.1146_1147insAAAGAAGAGAACTATGGCATA (ALOX12) MANE Select	ENSP00000251535.6:p.Leu382_His383insLysGluGluAsnTyrGlyIle
ENST00000251535.10:c.1146_1147insAAAGAAGAGAACTATGGCATA (ALOX12)	ENSP00000251535.6:p.Leu382_His383insLysGluGluAsnTyrGlyIle
NM_000697.2:c.1146_1147insAAAGAAGAGAACTATGGCATA (ALOX12)	NP_000688.2:p.Leu382_His383insLysGluGluAsnTyrGlyIle
NR_040089.1:n.233+7999_233+8000insTATGCCATAGTTCTCTTCTTT (ALOX12-AS1)
XM_011523780.1:c.1296_1297insAAAGAAGAGAACTATGGCATA (ALOX12)	XP_011522082.1:p.Leu432_His433insLysGluGluAsnTyrGlyIle
XM_011523780.2:c.1296_1297insAAAGAAGAGAACTATGGCATA (ALOX12)	XP_011522082.1:p.Leu432_His433insLysGluGluAsnTyrGlyIle
NM_000697.3:c.1146_1147insAAAGAAGAGAACTATGGCATA (ALOX12) MANE Select	NP_000688.2:p.Leu382_His383insLysGluGluAsnTyrGlyIle