Canonical Allele Identifier: CA2003456956
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339710A= , CM000673.2:g.118339710A= GRCh38
NC_000011.9:g.118210425A= , CM000673.1:g.118210425A= GRCh37
NC_000011.8:g.117715635A= NCBI36
NG_007566.1:g.367A= , LRG_39:g.367A=
NG_009891.1:g.8035T= , LRG_37:g.8035T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.958T=
ENST00000695667.1:n.476T=
ENST00000300692.9:c.406+65T= MANE Select ENSP00000300692.4:n.406+65T=
ENST00000300692.8:c.406+65T= ENSP00000300692.4:n.406+65T=
ENST00000392884.2:c.275-216T= ENSP00000376622.2:n.275-216T=
ENST00000526561.1:n.80-216T=
ENST00000529594.5:c.187+65T= ENSP00000437335.1:n.187+65T=
ENST00000534687.5:c.288-216T=
NM_000732.4:c.406+65T= , LRG_37t1:c.406+65T= NP_000723.1:n.406+65T=
NM_001040651.1:c.275-216T= NP_001035741.1:n.275-216T=
NM_001040651.2:c.275-216T= NP_001035741.1:n.275-216T=
NM_000732.6:c.406+65T= MANE Select NP_000723.1:n.406+65T=