Canonical Allele Identifier: CA774565150
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1361063839
MyVariant Identifiers: chr17:g.6899936_6899937insCA (hg19) chr17:g.6996617_6996618insCA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996618_6996619dup , CM000679.2:g.6996618_6996619dup GRCh38
NC_000017.10:g.6899937_6899938dup , CM000679.1:g.6899937_6899938dup GRCh37
NC_000017.9:g.6840661_6840662dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.136-208_136-207dup (ALOX12) MANE Select ENSP00000251535.6:n.136-208_136-207dup
ENST00000251535.10:c.136-208_136-207dup (ALOX12) ENSP00000251535.6:n.136-208_136-207dup
NM_000697.2:c.136-208_136-207dup (ALOX12) NP_000688.2:n.136-208_136-207dup
NR_040089.1:n.234-11079_234-11078dup (ALOX12-AS1)
XM_011523780.1:c.493-208_493-207dup (ALOX12) XP_011522082.1:n.493-208_493-207dup
XM_011523780.2:c.493-208_493-207dup (ALOX12) XP_011522082.1:n.493-208_493-207dup
NM_000697.3:c.136-208_136-207dup (ALOX12) MANE Select NP_000688.2:n.136-208_136-207dup
Search 100 bp 5'
Search 100 bp 3'