Canonical Allele Identifier: CA2003457136

Gene: CD3D

Linked Data

• dbSNP Id: rs1948286145

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118340026del , CM000673.2:g.118340026del	GRCh38
NC_000011.9:g.118210741del , CM000673.1:g.118210741del	GRCh37
NC_000011.8:g.117715951del	NCBI36
NG_007566.1:g.683del , LRG_39:g.683del
NG_009891.1:g.7719del , LRG_37:g.7719del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.642del
ENST00000695667.1:n.280-120del
ENST00000695668.1:n.2260-120del
ENST00000300692.9:c.275-120del MANE Select	ENSP00000300692.4:n.275-120del
ENST00000300692.8:c.275-120del	ENSP00000300692.4:n.275-120del
ENST00000392884.2:c.274+349del	ENSP00000376622.2:n.274+349del
ENST00000526561.1:n.80-532del
ENST00000529594.5:c.56-120del	ENSP00000437335.1:n.56-120del
ENST00000534687.5:c.287+349del
NM_000732.4:c.275-120del , LRG_37t1:c.275-120del	NP_000723.1:n.275-120del
NM_001040651.1:c.274+349del	NP_001035741.1:n.274+349del
NM_001040651.2:c.274+349del	NP_001035741.1:n.274+349del
NM_000732.6:c.275-120del MANE Select	NP_000723.1:n.275-120del