Canonical Allele Identifier: CA2003457038
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339805C= , CM000673.2:g.118339805C= GRCh38
NC_000011.9:g.118210520C= , CM000673.1:g.118210520C= GRCh37
NC_000011.8:g.117715730C= NCBI36
NG_007566.1:g.462C= , LRG_39:g.462C=
NG_009891.1:g.7940G= , LRG_37:g.7940G=

Transcript Alleles

HGVS Amino-acid change
ENST00000695666.1:n.863G=
ENST00000695667.1:n.381G=
ENST00000695668.1:n.2361G=
ENST00000300692.9:c.376G= MANE Select ENSP00000300692.4:p.Ala126=
ENST00000300692.8:c.376G= ENSP00000300692.4:p.Ala126=
ENST00000392884.2:c.275-311G= ENSP00000376622.2:n.275-311G=
ENST00000526561.1:n.80-311G=
ENST00000529594.5:c.157G= ENSP00000437335.1:p.Ala53=
ENST00000534687.5:c.288-311G=
NM_000732.4:c.376G= , LRG_37t1:c.376G= NP_000723.1:p.Ala126=
NM_001040651.1:c.275-311G= NP_001035741.1:n.275-311G=
NM_001040651.2:c.275-311G= NP_001035741.1:n.275-311G=
NM_000732.6:c.376G= MANE Select NP_000723.1:p.Ala126=