Canonical Allele Identifier: CA2741213813
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118340138G>A , CM000673.2:g.118340138G>A GRCh38
NC_000011.9:g.118210853G>A , CM000673.1:g.118210853G>A GRCh37
NC_000011.8:g.117716063G>A NCBI36
NG_007566.1:g.795G>A , LRG_39:g.795G>A
NG_009891.1:g.7607C>T , LRG_37:g.7607C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.530C>T
ENST00000695667.1:n.280-232C>T
ENST00000695668.1:n.2260-232C>T
ENST00000300692.9:c.275-232C>T MANE Select ENSP00000300692.4:n.275-232C>T
ENST00000300692.8:c.275-232C>T ENSP00000300692.4:n.275-232C>T
ENST00000392884.2:c.274+237C>T ENSP00000376622.2:n.274+237C>T
ENST00000526561.1:n.80-644C>T
ENST00000529594.5:c.56-232C>T ENSP00000437335.1:n.56-232C>T
ENST00000534687.5:c.287+237C>T
NM_000732.4:c.275-232C>T , LRG_37t1:c.275-232C>T NP_000723.1:n.275-232C>T
NM_001040651.1:c.274+237C>T NP_001035741.1:n.274+237C>T
NM_001040651.2:c.274+237C>T NP_001035741.1:n.274+237C>T
NM_000732.6:c.275-232C>T MANE Select NP_000723.1:n.275-232C>T