Canonical Allele Identifier: CA2003457008

Gene: CD3D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339754_118339756delinsATG , CM000673.2:g.118339754_118339756delinsATG	GRCh38
NC_000011.9:g.118210469_118210471delinsATG , CM000673.1:g.118210469_118210471delinsATG	GRCh37
NC_000011.8:g.117715679_117715681delinsATG	NCBI36
NG_007566.1:g.411_413delinsATG , LRG_39:g.411_413delinsATG
NG_009891.1:g.7989_7991delinsCAT , LRG_37:g.7989_7991delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.912_914delinsCAT
ENST00000695667.1:n.430_432delinsCAT
ENST00000695668.1:n.2410_2412delinsCAT
ENST00000300692.9:c.406+19_406+21delinsCAT MANE Select	ENSP00000300692.4:n.406+19_406+21delinsCAT
ENST00000300692.8:c.406+19_406+21delinsCAT	ENSP00000300692.4:n.406+19_406+21delinsCAT
ENST00000392884.2:c.275-262_275-260delinsCAT	ENSP00000376622.2:n.275-262_275-260delinsCAT
ENST00000526561.1:n.80-262_80-260delinsCAT
ENST00000529594.5:c.187+19_187+21delinsCAT	ENSP00000437335.1:n.187+19_187+21delinsCAT
ENST00000534687.5:c.288-262_288-260delinsCAT
NM_000732.4:c.406+19_406+21delinsCAT , LRG_37t1:c.406+19_406+21delinsCAT	NP_000723.1:n.406+19_406+21delinsCAT
NM_001040651.1:c.275-262_275-260delinsCAT	NP_001035741.1:n.275-262_275-260delinsCAT
NM_001040651.2:c.275-262_275-260delinsCAT	NP_001035741.1:n.275-262_275-260delinsCAT
NM_000732.6:c.406+19_406+21delinsCAT MANE Select	NP_000723.1:n.406+19_406+21delinsCAT