Canonical Allele Identifier: CA2003457079
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339915G= , CM000673.2:g.118339915G= GRCh38
NC_000011.9:g.118210630G= , CM000673.1:g.118210630G= GRCh37
NC_000011.8:g.117715840G= NCBI36
NG_007566.1:g.572G= , LRG_39:g.572G=
NG_009891.1:g.7830C= , LRG_37:g.7830C=

Transcript Alleles

HGVS Amino-acid change
ENST00000695666.1:n.753C=
ENST00000695667.1:n.280-9C=
ENST00000695668.1:n.2260-9C=
ENST00000300692.9:c.275-9C= MANE Select ENSP00000300692.4:n.275-9C=
ENST00000300692.8:c.275-9C= ENSP00000300692.4:n.275-9C=
ENST00000392884.2:c.275-421C= ENSP00000376622.2:n.275-421C=
ENST00000526561.1:n.80-421C=
ENST00000529594.5:c.56-9C= ENSP00000437335.1:n.56-9C=
ENST00000534687.5:c.288-421C=
NM_000732.4:c.275-9C= , LRG_37t1:c.275-9C= NP_000723.1:n.275-9C=
NM_001040651.1:c.275-421C= NP_001035741.1:n.275-421C=
NM_001040651.2:c.275-421C= NP_001035741.1:n.275-421C=
NM_000732.6:c.275-9C= MANE Select NP_000723.1:n.275-9C=