Canonical Allele Identifier: CA2637660876

Gene: ORMDL3

Linked Data

• gnomAD v4: 17-39926490-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39926490C>T , CM000679.2:g.39926490C>T	GRCh38
NC_000017.10:g.38082743C>T , CM000679.1:g.38082743C>T	GRCh37
NC_000017.9:g.35336269C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000304046.7:c.-23+994G>A MANE Select	ENSP00000304858.2:n.-23+994G>A
ENST00000304046.6:c.-23+994G>A	ENSP00000304858.2:n.-23+994G>A
ENST00000394169.5:c.-1144G>A	ENSP00000377724.1:n.-1144G>A
ENST00000579695.5:c.-18+994G>A	ENSP00000464693.1:n.-18+994G>A
ENST00000582052.1:n.31-151G>A
ENST00000584000.1:c.-23+577G>A	ENSP00000464298.1:n.-23+577G>A
NM_139280.2:c.-23+994G>A	NP_644809.1:n.-23+994G>A
XM_005257825.3:c.-23+327G>A	XP_005257882.2:n.-23+327G>A
XM_005257827.2:c.-18+994G>A	XP_005257884.1:n.-18+994G>A
NM_001320801.1:c.-1144G>A	NP_001307730.1:n.-1144G>A
NM_001320802.1:c.-18+994G>A	NP_001307731.1:n.-18+994G>A
NM_001320803.1:c.-23+327G>A	NP_001307732.1:n.-23+327G>A
NM_139280.3:c.-23+994G>A	NP_644809.1:n.-23+994G>A
NM_139280.4:c.-23+994G>A MANE Select	NP_644809.1:n.-23+994G>A
NM_001320802.2:c.-18+994G>A	NP_001307731.1:n.-18+994G>A
NM_001320801.2:c.-1144G>A	NP_001307730.1:n.-1144G>A