Canonical Allele Identifier: CA2245576067
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001577_7001580delinsGTTC , CM000679.2:g.7001577_7001580delinsGTTC GRCh38
NC_000017.10:g.6904896_6904899delinsGTTC , CM000679.1:g.6904896_6904899delinsGTTC GRCh37
NC_000017.9:g.6845620_6845623delinsGTTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.952-25_952-22delinsGTTC (ALOX12) MANE Select ENSP00000251535.6:n.952-25_952-22delinsGTTC
ENST00000251535.10:c.952-25_952-22delinsGTTC (ALOX12) ENSP00000251535.6:n.952-25_952-22delinsGTTC
NM_000697.2:c.952-25_952-22delinsGTTC (ALOX12) NP_000688.2:n.952-25_952-22delinsGTTC
NR_040089.1:n.233+8216_233+8219delinsGAAC (ALOX12-AS1)
XM_011523780.1:c.1102-25_1102-22delinsGTTC (ALOX12) XP_011522082.1:n.1102-25_1102-22delinsGTTC
XM_011523780.2:c.1102-25_1102-22delinsGTTC (ALOX12) XP_011522082.1:n.1102-25_1102-22delinsGTTC
NM_000697.3:c.952-25_952-22delinsGTTC (ALOX12) MANE Select NP_000688.2:n.952-25_952-22delinsGTTC