Canonical Allele Identifier: CA624675767
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1396715151
gnomAD v2: 17-6900056-CTG-C
gnomAD v3: 17-6996737-CTG-C
gnomAD v4: 17-6996737-CTG-C
MyVariant Identifiers: chr17:g.6900057_6900058del (hg19) chr17:g.6996738_6996739del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996738_6996739del , CM000679.2:g.6996738_6996739del GRCh38
NC_000017.10:g.6900057_6900058del , CM000679.1:g.6900057_6900058del GRCh37
NC_000017.9:g.6840781_6840782del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.136-88_136-87del (ALOX12) MANE Select ENSP00000251535.6:n.136-88_136-87del
ENST00000251535.10:c.136-88_136-87del (ALOX12) ENSP00000251535.6:n.136-88_136-87del
NM_000697.2:c.136-88_136-87del (ALOX12) NP_000688.2:n.136-88_136-87del
NR_040089.1:n.234-11199_234-11198del (ALOX12-AS1)
XM_011523780.1:c.493-88_493-87del (ALOX12) XP_011522082.1:n.493-88_493-87del
XM_011523780.2:c.493-88_493-87del (ALOX12) XP_011522082.1:n.493-88_493-87del
NM_000697.3:c.136-88_136-87del (ALOX12) MANE Select NP_000688.2:n.136-88_136-87del
Search 100 bp 5'
Search 100 bp 3'