Canonical Allele Identifier: CA397749076
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

COSMIC: COSM1679443
MyVariant Identifiers: chr17:g.6905110G>A (hg19) chr17:g.7001791G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001791G>A , CM000679.2:g.7001791G>A GRCh38
NC_000017.10:g.6905110G>A , CM000679.1:g.6905110G>A GRCh37
NC_000017.9:g.6845834G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1141G>A (ALOX12) MANE Select ENSP00000251535.6:p.Gly381Arg
ENST00000251535.10:c.1141G>A (ALOX12) ENSP00000251535.6:p.Gly381Arg
NM_000697.2:c.1141G>A (ALOX12) NP_000688.2:p.Gly381Arg
NR_040089.1:n.233+8005C>T (ALOX12-AS1)
XM_011523780.1:c.1291G>A (ALOX12) XP_011522082.1:p.Gly431Arg
XM_011523780.2:c.1291G>A (ALOX12) XP_011522082.1:p.Gly431Arg
NM_000697.3:c.1141G>A (ALOX12) MANE Select NP_000688.2:p.Gly381Arg
Search 100 bp 5'
Search 100 bp 3'