Canonical Allele Identifier: CA2635746112
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6997018del , CM000679.2:g.6997018del GRCh38
NC_000017.10:g.6900337del , CM000679.1:g.6900337del GRCh37
NC_000017.9:g.6841061del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.328del (ALOX12) MANE Select ENSP00000251535.6:p.Glu110ArgfsTer23
ENST00000251535.10:c.328del (ALOX12) ENSP00000251535.6:p.Glu110ArgfsTer23
ENST00000480801.1:c.37del (ALOX12) ENSP00000467033.1:p.Glu13ArgfsTer23
NM_000697.2:c.328del (ALOX12) NP_000688.2:p.Glu110ArgfsTer23
NR_040089.1:n.234-11478del (ALOX12-AS1)
XM_011523780.1:c.685del (ALOX12) XP_011522082.1:p.Glu229ArgfsTer23
XM_011523780.2:c.685del (ALOX12) XP_011522082.1:p.Glu229ArgfsTer23
NM_000697.3:c.328del (ALOX12) MANE Select NP_000688.2:p.Glu110ArgfsTer23