Canonical Allele Identifier: CA2003457001
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339749C= , CM000673.2:g.118339749C= GRCh38
NC_000011.9:g.118210464C= , CM000673.1:g.118210464C= GRCh37
NC_000011.8:g.117715674C= NCBI36
NG_007566.1:g.406C= , LRG_39:g.406C=
NG_009891.1:g.7996G= , LRG_37:g.7996G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.919G=
ENST00000695667.1:n.437G=
ENST00000695668.1:n.2417G=
ENST00000300692.9:c.406+26G= MANE Select ENSP00000300692.4:n.406+26G=
ENST00000300692.8:c.406+26G= ENSP00000300692.4:n.406+26G=
ENST00000392884.2:c.275-255G= ENSP00000376622.2:n.275-255G=
ENST00000526561.1:n.80-255G=
ENST00000529594.5:c.187+26G= ENSP00000437335.1:n.187+26G=
ENST00000534687.5:c.288-255G=
NM_000732.4:c.406+26G= , LRG_37t1:c.406+26G= NP_000723.1:n.406+26G=
NM_001040651.1:c.275-255G= NP_001035741.1:n.275-255G=
NM_001040651.2:c.275-255G= NP_001035741.1:n.275-255G=
NM_000732.6:c.406+26G= MANE Select NP_000723.1:n.406+26G=