Canonical Allele Identifier: CA2637660827

Gene: ORMDL3

Linked Data

• gnomAD v4: 17-39926398-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39926398A>G , CM000679.2:g.39926398A>G	GRCh38
NC_000017.10:g.38082651A>G , CM000679.1:g.38082651A>G	GRCh37
NC_000017.9:g.35336177A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000304046.7:c.-23+1086T>C MANE Select	ENSP00000304858.2:n.-23+1086T>C
ENST00000304046.6:c.-23+1086T>C	ENSP00000304858.2:n.-23+1086T>C
ENST00000394169.5:c.-1052T>C	ENSP00000377724.1:n.-1052T>C
ENST00000579695.5:c.-18+1086T>C	ENSP00000464693.1:n.-18+1086T>C
ENST00000582052.1:n.31-59T>C
ENST00000584000.1:c.-23+669T>C	ENSP00000464298.1:n.-23+669T>C
NM_139280.2:c.-23+1086T>C	NP_644809.1:n.-23+1086T>C
XM_005257825.3:c.-23+419T>C	XP_005257882.2:n.-23+419T>C
XM_005257827.2:c.-18+1086T>C	XP_005257884.1:n.-18+1086T>C
NM_001320801.1:c.-1052T>C	NP_001307730.1:n.-1052T>C
NM_001320802.1:c.-18+1086T>C	NP_001307731.1:n.-18+1086T>C
NM_001320803.1:c.-23+419T>C	NP_001307732.1:n.-23+419T>C
NM_139280.3:c.-23+1086T>C	NP_644809.1:n.-23+1086T>C
NM_139280.4:c.-23+1086T>C MANE Select	NP_644809.1:n.-23+1086T>C
NM_001320802.2:c.-18+1086T>C	NP_001307731.1:n.-18+1086T>C
NM_001320801.2:c.-1052T>C	NP_001307730.1:n.-1052T>C