Canonical Allele Identifier: CA2635747809

Gene: ALOX12 ALOX12-AS1

Linked Data

• gnomAD v4: 17-7001900-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7001900C>A , CM000679.2:g.7001900C>A	GRCh38
NC_000017.10:g.6905219C>A , CM000679.1:g.6905219C>A	GRCh37
NC_000017.9:g.6845943C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.1161+89C>A (ALOX12) MANE Select	ENSP00000251535.6:n.1161+89C>A
ENST00000251535.10:c.1161+89C>A (ALOX12)	ENSP00000251535.6:n.1161+89C>A
NM_000697.2:c.1161+89C>A (ALOX12)	NP_000688.2:n.1161+89C>A
NR_040089.1:n.233+7896G>T (ALOX12-AS1)
XM_011523780.1:c.1311+89C>A (ALOX12)	XP_011522082.1:n.1311+89C>A
XM_011523780.2:c.1311+89C>A (ALOX12)	XP_011522082.1:n.1311+89C>A
NM_000697.3:c.1161+89C>A (ALOX12) MANE Select	NP_000688.2:n.1161+89C>A