Canonical Allele Identifier: CA2259314309
Gene: ORMDL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39926562T= , CM000679.2:g.39926562T= GRCh38
NC_000017.10:g.38082815T= , CM000679.1:g.38082815T= GRCh37
NC_000017.9:g.35336341T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000304046.7:c.-23+922A= MANE Select ENSP00000304858.2:n.-23+922A=
ENST00000304046.6:c.-23+922A= ENSP00000304858.2:n.-23+922A=
ENST00000394169.5:c.-1216A= ENSP00000377724.1:n.-1216A=
ENST00000579695.5:c.-18+922A= ENSP00000464693.1:n.-18+922A=
ENST00000582052.1:n.31-223A=
ENST00000584000.1:c.-23+505A= ENSP00000464298.1:n.-23+505A=
NM_139280.2:c.-23+922A= NP_644809.1:n.-23+922A=
XM_005257825.3:c.-23+255A= XP_005257882.2:n.-23+255A=
XM_005257827.2:c.-18+922A= XP_005257884.1:n.-18+922A=
NM_001320801.1:c.-1216A= NP_001307730.1:n.-1216A=
NM_001320802.1:c.-18+922A= NP_001307731.1:n.-18+922A=
NM_001320803.1:c.-23+255A= NP_001307732.1:n.-23+255A=
NM_139280.3:c.-23+922A= NP_644809.1:n.-23+922A=
NM_139280.4:c.-23+922A= MANE Select NP_644809.1:n.-23+922A=
NM_001320802.2:c.-18+922A= NP_001307731.1:n.-18+922A=
NM_001320801.2:c.-1216A= NP_001307730.1:n.-1216A=