Canonical Allele Identifier: CA8333407

Gene: ALOX12 ALOX12-AS1

Linked Data

• dbSNP Id: rs138098217
• ExAC: 17:6905099 G / A
• gnomAD v2: 17-6905099-G-A
• gnomAD v3: 17-7001780-G-A
• gnomAD v4: 17-7001780-G-A
• MyVariant Identifiers: chr17:g.6905099G>A (hg19) ; chr17:g.7001780G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7001780G>A , CM000679.2:g.7001780G>A	GRCh38
NC_000017.10:g.6905099G>A , CM000679.1:g.6905099G>A	GRCh37
NC_000017.9:g.6845823G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.1130G>A (ALOX12) MANE Select	ENSP00000251535.6:p.Arg377Gln
ENST00000251535.10:c.1130G>A (ALOX12)	ENSP00000251535.6:p.Arg377Gln
NM_000697.2:c.1130G>A (ALOX12)	NP_000688.2:p.Arg377Gln
NR_040089.1:n.233+8016C>T (ALOX12-AS1)
XM_011523780.1:c.1280G>A (ALOX12)	XP_011522082.1:p.Arg427Gln
XM_011523780.2:c.1280G>A (ALOX12)	XP_011522082.1:p.Arg427Gln
NM_000697.3:c.1130G>A (ALOX12) MANE Select	NP_000688.2:p.Arg377Gln