Canonical Allele Identifier: CA2245576075
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001585_7001589delinsATTTC , CM000679.2:g.7001585_7001589delinsATTTC GRCh38
NC_000017.10:g.6904904_6904908delinsATTTC , CM000679.1:g.6904904_6904908delinsATTTC GRCh37
NC_000017.9:g.6845628_6845632delinsATTTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.952-17_952-13delinsATTTC (ALOX12) MANE Select ENSP00000251535.6:n.952-17_952-13delinsATTTC
ENST00000251535.10:c.952-17_952-13delinsATTTC (ALOX12) ENSP00000251535.6:n.952-17_952-13delinsATTTC
NM_000697.2:c.952-17_952-13delinsATTTC (ALOX12) NP_000688.2:n.952-17_952-13delinsATTTC
NR_040089.1:n.233+8207_233+8211delinsGAAAT (ALOX12-AS1)
XM_011523780.1:c.1102-17_1102-13delinsATTTC (ALOX12) XP_011522082.1:n.1102-17_1102-13delinsATTTC
XM_011523780.2:c.1102-17_1102-13delinsATTTC (ALOX12) XP_011522082.1:n.1102-17_1102-13delinsATTTC
NM_000697.3:c.952-17_952-13delinsATTTC (ALOX12) MANE Select NP_000688.2:n.952-17_952-13delinsATTTC