Canonical Allele Identifier: CA2003456990

Gene: CD3D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339740A= , CM000673.2:g.118339740A=	GRCh38
NC_000011.9:g.118210455A= , CM000673.1:g.118210455A=	GRCh37
NC_000011.8:g.117715665A=	NCBI36
NG_007566.1:g.397A= , LRG_39:g.397A=
NG_009891.1:g.8005T= , LRG_37:g.8005T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.928T=
ENST00000695667.1:n.446T=
ENST00000695668.1:n.2426T=
ENST00000300692.9:c.406+35T= MANE Select	ENSP00000300692.4:n.406+35T=
ENST00000300692.8:c.406+35T=	ENSP00000300692.4:n.406+35T=
ENST00000392884.2:c.275-246T=	ENSP00000376622.2:n.275-246T=
ENST00000526561.1:n.80-246T=
ENST00000529594.5:c.187+35T=	ENSP00000437335.1:n.187+35T=
ENST00000534687.5:c.288-246T=
NM_000732.4:c.406+35T= , LRG_37t1:c.406+35T=	NP_000723.1:n.406+35T=
NM_001040651.1:c.275-246T=	NP_001035741.1:n.275-246T=
NM_001040651.2:c.275-246T=	NP_001035741.1:n.275-246T=
NM_000732.6:c.406+35T= MANE Select	NP_000723.1:n.406+35T=