Canonical Allele Identifier: CA2616232533

Gene: CD3D

Linked Data

• gnomAD v4: 11-118340223-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118340223T>G , CM000673.2:g.118340223T>G	GRCh38
NC_000011.9:g.118210938T>G , CM000673.1:g.118210938T>G	GRCh37
NC_000011.8:g.117716148T>G	NCBI36
NG_007566.1:g.880T>G , LRG_39:g.880T>G
NG_009891.1:g.7522A>C , LRG_37:g.7522A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.445A>C
ENST00000695667.1:n.279+152A>C
ENST00000695668.1:n.2259+152A>C
ENST00000300692.9:c.274+152A>C MANE Select	ENSP00000300692.4:n.274+152A>C
ENST00000300692.8:c.274+152A>C	ENSP00000300692.4:n.274+152A>C
ENST00000392884.2:c.274+152A>C	ENSP00000376622.2:n.274+152A>C
ENST00000526561.1:n.80-729A>C
ENST00000529594.5:c.56-317A>C	ENSP00000437335.1:n.56-317A>C
ENST00000534687.5:c.287+152A>C
NM_000732.4:c.274+152A>C , LRG_37t1:c.274+152A>C	NP_000723.1:n.274+152A>C
NM_001040651.1:c.274+152A>C	NP_001035741.1:n.274+152A>C
NM_001040651.2:c.274+152A>C	NP_001035741.1:n.274+152A>C
NM_000732.6:c.274+152A>C MANE Select	NP_000723.1:n.274+152A>C