Canonical Allele Identifier: CA2259314147
Gene: ORMDL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39926220C= , CM000679.2:g.39926220C= GRCh38
NC_000017.10:g.38082473C= , CM000679.1:g.38082473C= GRCh37
NC_000017.9:g.35335999C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000304046.7:c.-23+1264G= MANE Select ENSP00000304858.2:n.-23+1264G=
ENST00000304046.6:c.-23+1264G= ENSP00000304858.2:n.-23+1264G=
ENST00000394169.5:c.-874G= ENSP00000377724.1:n.-874G=
ENST00000579695.5:c.-18+1264G= ENSP00000464693.1:n.-18+1264G=
ENST00000582052.1:n.150G=
ENST00000584000.1:c.-23+847G= ENSP00000464298.1:n.-23+847G=
NM_139280.2:c.-23+1264G= NP_644809.1:n.-23+1264G=
XM_005257825.3:c.-23+597G= XP_005257882.2:n.-23+597G=
XM_005257827.2:c.-18+1264G= XP_005257884.1:n.-18+1264G=
NM_001320801.1:c.-874G= NP_001307730.1:n.-874G=
NM_001320802.1:c.-18+1264G= NP_001307731.1:n.-18+1264G=
NM_001320803.1:c.-23+597G= NP_001307732.1:n.-23+597G=
NM_139280.3:c.-23+1264G= NP_644809.1:n.-23+1264G=
NM_139280.4:c.-23+1264G= MANE Select NP_644809.1:n.-23+1264G=
NM_001320802.2:c.-18+1264G= NP_001307731.1:n.-18+1264G=
NM_001320801.2:c.-874G= NP_001307730.1:n.-874G=