Canonical Allele Identifier: CA397748831
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6905080A>T (hg19) chr17:g.7001761A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001761A>T , CM000679.2:g.7001761A>T GRCh38
NC_000017.10:g.6905080A>T , CM000679.1:g.6905080A>T GRCh37
NC_000017.9:g.6845804A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1111A>T (ALOX12) MANE Select ENSP00000251535.6:p.Ile371Phe
ENST00000251535.10:c.1111A>T (ALOX12) ENSP00000251535.6:p.Ile371Phe
NM_000697.2:c.1111A>T (ALOX12) NP_000688.2:p.Ile371Phe
NR_040089.1:n.233+8035T>A (ALOX12-AS1)
XM_011523780.1:c.1261A>T (ALOX12) XP_011522082.1:p.Ile421Phe
XM_011523780.2:c.1261A>T (ALOX12) XP_011522082.1:p.Ile421Phe
NM_000697.3:c.1111A>T (ALOX12) MANE Select NP_000688.2:p.Ile371Phe
Search 100 bp 5'
Search 100 bp 3'