Canonical Allele Identifier: CA2003457186

Gene: CD3D

Linked Data

• dbSNP Id: rs1948286983

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118340179_118340185dup , CM000673.2:g.118340179_118340185dup	GRCh38
NC_000011.9:g.118210894_118210900dup , CM000673.1:g.118210894_118210900dup	GRCh37
NC_000011.8:g.117716104_117716110dup	NCBI36
NG_007566.1:g.836_842dup , LRG_39:g.836_842dup
NG_009891.1:g.7560_7566dup , LRG_37:g.7560_7566dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.483_489dup
ENST00000695667.1:n.279+190_279+196dup
ENST00000695668.1:n.2259+190_2259+196dup
ENST00000300692.9:c.274+190_274+196dup MANE Select	ENSP00000300692.4:n.274+190_274+196dup
ENST00000300692.8:c.274+190_274+196dup	ENSP00000300692.4:n.274+190_274+196dup
ENST00000392884.2:c.274+190_274+196dup	ENSP00000376622.2:n.274+190_274+196dup
ENST00000526561.1:n.80-691_80-685dup
ENST00000529594.5:c.56-279_56-273dup	ENSP00000437335.1:n.56-279_56-273dup
ENST00000534687.5:c.287+190_287+196dup
NM_000732.4:c.274+190_274+196dup , LRG_37t1:c.274+190_274+196dup	NP_000723.1:n.274+190_274+196dup
NM_001040651.1:c.274+190_274+196dup	NP_001035741.1:n.274+190_274+196dup
NM_001040651.2:c.274+190_274+196dup	NP_001035741.1:n.274+190_274+196dup
NM_000732.6:c.274+190_274+196dup MANE Select	NP_000723.1:n.274+190_274+196dup