Canonical Allele Identifier: CA2246125360

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8075552_8075581delinsCAGTCCCAGCTCCCCCTGATTGCCCAGGTG , CM000679.2:g.8075552_8075581delinsCAGTCCCAGCTCCCCCTGATTGCCCAGGTG	GRCh38
NC_000017.10:g.7978870_7978899delinsCAGTCCCAGCTCCCCCTGATTGCCCAGGTG , CM000679.1:g.7978870_7978899delinsCAGTCCCAGCTCCCCCTGATTGCCCAGGTG	GRCh37
NC_000017.9:g.7919595_7919624delinsCAGTCCCAGCTCCCCCTGATTGCCCAGGTG	NCBI36
NG_007099.1:g.17123_17152delinsCACCTGGGCAATCAGGGGGAGCTGGGACTG
NG_007099.2:g.17136_17165delinsCACCTGGGCAATCAGGGGGAGCTGGGACTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1654+14_1654+43delinsCACCTGGGCAATCAGGGGGAGCTGGGACTG MANE Select	ENSP00000497784.1:n.1654+14_1654+43delinsCACCTGGGCAATCAGGGGGA...
ENST00000649809.1:c.718+14_718+43delinsCACCTGGGCAATCAGGGGGAGCTGGGACTG	ENSP00000496845.1:n.718+14_718+43delinsCACCTGGGCAATCAGGGGGAGC...
ENST00000319144.4:c.1654+14_1654+43delinsCACCTGGGCAATCAGGGGGAGCTGGGACTG	ENSP00000315167.4:n.1654+14_1654+43delinsCACCTGGGCAATCAGGGGGA...
ENST00000577351.5:n.479+594_479+623delinsCACCTGGGCAATCAGGGGGAGCTGGGACTG
NM_001139.2:c.1654+14_1654+43delinsCACCTGGGCAATCAGGGGGAGCTGGGACTG	NP_001130.1:n.1654+14_1654+43delinsCACCTGGGCAATCAGGGGGAGCTGGG...
NM_001139.3:c.1654+14_1654+43delinsCACCTGGGCAATCAGGGGGAGCTGGGACTG MANE Select	NP_001130.1:n.1654+14_1654+43delinsCACCTGGGCAATCAGGGGGAGCTGGG...