Canonical Allele Identifier: CA2574994335
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118340001C>A , CM000673.2:g.118340001C>A GRCh38
NC_000011.9:g.118210716C>A , CM000673.1:g.118210716C>A GRCh37
NC_000011.8:g.117715926C>A NCBI36
NG_007566.1:g.658C>A , LRG_39:g.658C>A
NG_009891.1:g.7744G>T , LRG_37:g.7744G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.667G>T
ENST00000695667.1:n.280-95G>T
ENST00000695668.1:n.2260-95G>T
ENST00000300692.9:c.275-95G>T MANE Select ENSP00000300692.4:n.275-95G>T
ENST00000300692.8:c.275-95G>T ENSP00000300692.4:n.275-95G>T
ENST00000392884.2:c.274+374G>T ENSP00000376622.2:n.274+374G>T
ENST00000526561.1:n.80-507G>T
ENST00000529594.5:c.56-95G>T ENSP00000437335.1:n.56-95G>T
ENST00000534687.5:c.287+374G>T
NM_000732.4:c.275-95G>T , LRG_37t1:c.275-95G>T NP_000723.1:n.275-95G>T
NM_001040651.1:c.274+374G>T NP_001035741.1:n.274+374G>T
NM_001040651.2:c.274+374G>T NP_001035741.1:n.274+374G>T
NM_000732.6:c.275-95G>T MANE Select NP_000723.1:n.275-95G>T