Canonical Allele Identifier: CA2637661010
Gene: ORMDL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39926583T>A , CM000679.2:g.39926583T>A GRCh38
NC_000017.10:g.38082836T>A , CM000679.1:g.38082836T>A GRCh37
NC_000017.9:g.35336362T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000304046.7:c.-23+901A>T MANE Select ENSP00000304858.2:n.-23+901A>T
ENST00000304046.6:c.-23+901A>T ENSP00000304858.2:n.-23+901A>T
ENST00000394169.5:c.-1237A>T ENSP00000377724.1:n.-1237A>T
ENST00000579695.5:c.-18+901A>T ENSP00000464693.1:n.-18+901A>T
ENST00000582052.1:n.30+234A>T
ENST00000584000.1:c.-23+484A>T ENSP00000464298.1:n.-23+484A>T
NM_139280.2:c.-23+901A>T NP_644809.1:n.-23+901A>T
XM_005257825.3:c.-23+234A>T XP_005257882.2:n.-23+234A>T
XM_005257827.2:c.-18+901A>T XP_005257884.1:n.-18+901A>T
NM_001320801.1:c.-1237A>T NP_001307730.1:n.-1237A>T
NM_001320802.1:c.-18+901A>T NP_001307731.1:n.-18+901A>T
NM_001320803.1:c.-23+234A>T NP_001307732.1:n.-23+234A>T
NM_139280.3:c.-23+901A>T NP_644809.1:n.-23+901A>T
NM_139280.4:c.-23+901A>T MANE Select NP_644809.1:n.-23+901A>T
NM_001320802.2:c.-18+901A>T NP_001307731.1:n.-18+901A>T
NM_001320801.2:c.-1237A>T NP_001307730.1:n.-1237A>T