Canonical Allele Identifier: CA382789092

Gene: CD3D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118340413T>C , CM000673.2:g.118340413T>C	GRCh38
NC_000011.9:g.118211128T>C , CM000673.1:g.118211128T>C	GRCh37
NC_000011.8:g.117716338T>C	NCBI36
NG_007566.1:g.1070T>C , LRG_39:g.1070T>C
NG_009891.1:g.7332A>G , LRG_37:g.7332A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000732.6:c.236A>G MANE Select	NP_000723.1:p.Tyr79Cys
ENST00000300692.9:c.236A>G MANE Select	ENSP00000300692.4:p.Tyr79Cys
NM_000732.4:c.236A>G , LRG_37t1:c.236A>G	NP_000723.1:p.Tyr79Cys
NM_001040651.1:c.236A>G	NP_001035741.1:p.Tyr79Cys
NM_001040651.2:c.236A>G	NP_001035741.1:p.Tyr79Cys
ENST00000300692.8:c.236A>G	ENSP00000300692.4:p.Tyr79Cys
ENST00000392884.2:c.236A>G	ENSP00000376622.2:p.Tyr79Cys
ENST00000526561.1:n.80-919A>G
ENST00000529594.5:c.56-507A>G	ENSP00000437335.1:n.56-507A>G
ENST00000534687.5:c.249A>G
ENST00000695666.1:n.255A>G
ENST00000695667.1:n.241A>G
ENST00000695668.1:n.2221A>G