Canonical Allele Identifier: CA2616232473

Gene: CD3D

Linked Data

• gnomAD v4: 11-118339982-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339982A>C , CM000673.2:g.118339982A>C	GRCh38
NC_000011.9:g.118210697A>C , CM000673.1:g.118210697A>C	GRCh37
NC_000011.8:g.117715907A>C	NCBI36
NG_007566.1:g.639A>C , LRG_39:g.639A>C
NG_009891.1:g.7763T>G , LRG_37:g.7763T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.686T>G
ENST00000695667.1:n.280-76T>G
ENST00000695668.1:n.2260-76T>G
ENST00000300692.9:c.275-76T>G MANE Select	ENSP00000300692.4:n.275-76T>G
ENST00000300692.8:c.275-76T>G	ENSP00000300692.4:n.275-76T>G
ENST00000392884.2:c.274+393T>G	ENSP00000376622.2:n.274+393T>G
ENST00000526561.1:n.80-488T>G
ENST00000529594.5:c.56-76T>G	ENSP00000437335.1:n.56-76T>G
ENST00000534687.5:c.287+393T>G
NM_000732.4:c.275-76T>G , LRG_37t1:c.275-76T>G	NP_000723.1:n.275-76T>G
NM_001040651.1:c.274+393T>G	NP_001035741.1:n.274+393T>G
NM_001040651.2:c.274+393T>G	NP_001035741.1:n.274+393T>G
NM_000732.6:c.275-76T>G MANE Select	NP_000723.1:n.275-76T>G