Canonical Allele Identifier: CA397738042

Gene: ALOX12 ALOX12-AS1

Linked Data

• gnomAD v4: 17-6996974-C-G
• MyVariant Identifiers: chr17:g.6900293C>G (hg19) ; chr17:g.6996974C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6996974C>G , CM000679.2:g.6996974C>G	GRCh38
NC_000017.10:g.6900293C>G , CM000679.1:g.6900293C>G	GRCh37
NC_000017.9:g.6841017C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.284C>G (ALOX12) MANE Select	ENSP00000251535.6:p.Pro95Arg
ENST00000251535.10:c.284C>G (ALOX12)	ENSP00000251535.6:p.Pro95Arg
NM_000697.2:c.284C>G (ALOX12)	NP_000688.2:p.Pro95Arg
NR_040089.1:n.234-11434G>C (ALOX12-AS1)
XM_011523780.1:c.641C>G (ALOX12)	XP_011522082.1:p.Pro214Arg
XM_011523780.2:c.641C>G (ALOX12)	XP_011522082.1:p.Pro214Arg
NM_000697.3:c.284C>G (ALOX12) MANE Select	NP_000688.2:p.Pro95Arg