Canonical Allele Identifier: CA382788505

Gene: CD3D

Linked Data

• MyVariant Identifiers: chr11:g.118210621A>C (hg19) ; chr11:g.118339906A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339906A>C , CM000673.2:g.118339906A>C	GRCh38
NC_000011.9:g.118210621A>C , CM000673.1:g.118210621A>C	GRCh37
NC_000011.8:g.117715831A>C	NCBI36
NG_007566.1:g.563A>C , LRG_39:g.563A>C
NG_009891.1:g.7839T>G , LRG_37:g.7839T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.762T>G
ENST00000695667.1:n.280T>G
ENST00000695668.1:n.2260T>G
ENST00000300692.9:c.275T>G MANE Select	ENSP00000300692.4:p.Met92Arg
ENST00000300692.8:c.275T>G	ENSP00000300692.4:p.Met92Arg
ENST00000392884.2:c.275-412T>G	ENSP00000376622.2:n.275-412T>G
ENST00000526561.1:n.80-412T>G
ENST00000529594.5:c.56T>G	ENSP00000437335.1:p.Val19Gly
ENST00000534687.5:c.288-412T>G
NM_000732.4:c.275T>G , LRG_37t1:c.275T>G	NP_000723.1:p.Met92Arg
NM_001040651.1:c.275-412T>G	NP_001035741.1:n.275-412T>G
NM_001040651.2:c.275-412T>G	NP_001035741.1:n.275-412T>G
NM_000732.6:c.275T>G MANE Select	NP_000723.1:p.Met92Arg