Canonical Allele Identifier: CA2793810960

Gene: CD3D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339840_118339854dup , CM000673.2:g.118339840_118339854dup	GRCh38
NC_000011.9:g.118210555_118210569dup , CM000673.1:g.118210555_118210569dup	GRCh37
NC_000011.8:g.117715765_117715779dup	NCBI36
NG_007566.1:g.497_511dup , LRG_39:g.497_511dup
NG_009891.1:g.7895_7909dup , LRG_37:g.7895_7909dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.818_832dup
ENST00000695667.1:n.336_350dup
ENST00000695668.1:n.2316_2330dup
ENST00000300692.9:c.331_345dup MANE Select	ENSP00000300692.4:p.Thr115_Leu116insAspValIleAlaThr
ENST00000300692.8:c.331_345dup	ENSP00000300692.4:p.Thr115_Leu116insAspValIleAlaThr
ENST00000392884.2:c.275-356_275-342dup	ENSP00000376622.2:n.275-356_275-342dup
ENST00000526561.1:n.80-356_80-342dup
ENST00000529594.5:c.112_126dup	ENSP00000437335.1:p.Thr42_Leu43insAspValIleAlaThr
ENST00000534687.5:c.288-356_288-342dup
NM_000732.4:c.331_345dup , LRG_37t1:c.331_345dup	NP_000723.1:p.Thr115_Leu116insAspValIleAlaThr
NM_001040651.1:c.275-356_275-342dup	NP_001035741.1:n.275-356_275-342dup
NM_001040651.2:c.275-356_275-342dup	NP_001035741.1:n.275-356_275-342dup
NM_000732.6:c.331_345dup MANE Select	NP_000723.1:p.Thr115_Leu116insAspValIleAlaThr