Canonical Allele Identifier: CA397749189
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v4: 17-7001801-C-T
MyVariant Identifiers: chr17:g.6905120C>T (hg19) chr17:g.7001801C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001801C>T , CM000679.2:g.7001801C>T GRCh38
NC_000017.10:g.6905120C>T , CM000679.1:g.6905120C>T GRCh37
NC_000017.9:g.6845844C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1151C>T (ALOX12) MANE Select ENSP00000251535.6:p.Pro384Leu
ENST00000251535.10:c.1151C>T (ALOX12) ENSP00000251535.6:p.Pro384Leu
NM_000697.2:c.1151C>T (ALOX12) NP_000688.2:p.Pro384Leu
NR_040089.1:n.233+7995G>A (ALOX12-AS1)
XM_011523780.1:c.1301C>T (ALOX12) XP_011522082.1:p.Pro434Leu
XM_011523780.2:c.1301C>T (ALOX12) XP_011522082.1:p.Pro434Leu
NM_000697.3:c.1151C>T (ALOX12) MANE Select NP_000688.2:p.Pro384Leu
Search 100 bp 5'
Search 100 bp 3'