Canonical Allele Identifier: CA397738294
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1475035058
gnomAD v4: 17-6997006-C-A
MyVariant Identifiers: chr17:g.6900325C>A (hg19) chr17:g.6997006C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6997006C>A , CM000679.2:g.6997006C>A GRCh38
NC_000017.10:g.6900325C>A , CM000679.1:g.6900325C>A GRCh37
NC_000017.9:g.6841049C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.316C>A (ALOX12) MANE Select ENSP00000251535.6:p.Leu106Met
ENST00000251535.10:c.316C>A (ALOX12) ENSP00000251535.6:p.Leu106Met
ENST00000480801.1:c.25C>A (ALOX12) ENSP00000467033.1:p.Leu9Met
NM_000697.2:c.316C>A (ALOX12) NP_000688.2:p.Leu106Met
NR_040089.1:n.234-11466G>T (ALOX12-AS1)
XM_011523780.1:c.673C>A (ALOX12) XP_011522082.1:p.Leu225Met
XM_011523780.2:c.673C>A (ALOX12) XP_011522082.1:p.Leu225Met
NM_000697.3:c.316C>A (ALOX12) MANE Select NP_000688.2:p.Leu106Met
Search 100 bp 5'
Search 100 bp 3'