Canonical Allele Identifier: CA397749099
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6905111G>T (hg19) chr17:g.7001792G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001792G>T , CM000679.2:g.7001792G>T GRCh38
NC_000017.10:g.6905111G>T , CM000679.1:g.6905111G>T GRCh37
NC_000017.9:g.6845835G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1142G>T (ALOX12) MANE Select ENSP00000251535.6:p.Gly381Val
ENST00000251535.10:c.1142G>T (ALOX12) ENSP00000251535.6:p.Gly381Val
NM_000697.2:c.1142G>T (ALOX12) NP_000688.2:p.Gly381Val
NR_040089.1:n.233+8004C>A (ALOX12-AS1)
XM_011523780.1:c.1292G>T (ALOX12) XP_011522082.1:p.Gly431Val
XM_011523780.2:c.1292G>T (ALOX12) XP_011522082.1:p.Gly431Val
NM_000697.3:c.1142G>T (ALOX12) MANE Select NP_000688.2:p.Gly381Val
Search 100 bp 5'
Search 100 bp 3'