Canonical Allele Identifier: CA2245576234
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001954_7001955delinsAT , CM000679.2:g.7001954_7001955delinsAT GRCh38
NC_000017.10:g.6905273_6905274delinsAT , CM000679.1:g.6905273_6905274delinsAT GRCh37
NC_000017.9:g.6845997_6845998delinsAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1161+143_1161+144delinsAT (ALOX12) MANE Select ENSP00000251535.6:n.1161+143_1161+144delinsAT
ENST00000251535.10:c.1161+143_1161+144delinsAT (ALOX12) ENSP00000251535.6:n.1161+143_1161+144delinsAT
NM_000697.2:c.1161+143_1161+144delinsAT (ALOX12) NP_000688.2:n.1161+143_1161+144delinsAT
NR_040089.1:n.233+7841_233+7842delinsAT (ALOX12-AS1)
XM_011523780.1:c.1311+143_1311+144delinsAT (ALOX12) XP_011522082.1:n.1311+143_1311+144delinsAT
XM_011523780.2:c.1311+143_1311+144delinsAT (ALOX12) XP_011522082.1:n.1311+143_1311+144delinsAT
NM_000697.3:c.1161+143_1161+144delinsAT (ALOX12) MANE Select NP_000688.2:n.1161+143_1161+144delinsAT