Canonical Allele Identifier: CA2245576208
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001919_7001924delinsTGAAGA , CM000679.2:g.7001919_7001924delinsTGAAGA GRCh38
NC_000017.10:g.6905238_6905243delinsTGAAGA , CM000679.1:g.6905238_6905243delinsTGAAGA GRCh37
NC_000017.9:g.6845962_6845967delinsTGAAGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1161+108_1161+113delinsTGAAGA (ALOX12) MANE Select ENSP00000251535.6:n.1161+108_1161+113delinsTGAAGA
ENST00000251535.10:c.1161+108_1161+113delinsTGAAGA (ALOX12) ENSP00000251535.6:n.1161+108_1161+113delinsTGAAGA
NM_000697.2:c.1161+108_1161+113delinsTGAAGA (ALOX12) NP_000688.2:n.1161+108_1161+113delinsTGAAGA
NR_040089.1:n.233+7872_233+7877delinsTCTTCA (ALOX12-AS1)
XM_011523780.1:c.1311+108_1311+113delinsTGAAGA (ALOX12) XP_011522082.1:n.1311+108_1311+113delinsTGAAGA
XM_011523780.2:c.1311+108_1311+113delinsTGAAGA (ALOX12) XP_011522082.1:n.1311+108_1311+113delinsTGAAGA
NM_000697.3:c.1161+108_1161+113delinsTGAAGA (ALOX12) MANE Select NP_000688.2:n.1161+108_1161+113delinsTGAAGA