Canonical Allele Identifier: CA2246125138

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8075370_8075371delinsGA , CM000679.2:g.8075370_8075371delinsGA	GRCh38
NC_000017.10:g.7978688_7978689delinsGA , CM000679.1:g.7978688_7978689delinsGA	GRCh37
NC_000017.9:g.7919413_7919414delinsGA	NCBI36
NG_007099.1:g.17333_17334delinsTC
NG_007099.2:g.17346_17347delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1654+224_1654+225delinsTC MANE Select	ENSP00000497784.1:n.1654+224_1654+225delinsTC
ENST00000649809.1:c.718+224_718+225delinsTC	ENSP00000496845.1:n.718+224_718+225delinsTC
ENST00000319144.4:c.1654+224_1654+225delinsTC	ENSP00000315167.4:n.1654+224_1654+225delinsTC
ENST00000577351.5:n.479+804_479+805delinsTC
NM_001139.2:c.1654+224_1654+225delinsTC	NP_001130.1:n.1654+224_1654+225delinsTC
NM_001139.3:c.1654+224_1654+225delinsTC MANE Select	NP_001130.1:n.1654+224_1654+225delinsTC