Canonical Allele Identifier: CA382788165

Gene: CD3D

Linked Data

• MyVariant Identifiers: chr11:g.118210529A>C (hg19) ; chr11:g.118339814A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339814A>C , CM000673.2:g.118339814A>C	GRCh38
NC_000011.9:g.118210529A>C , CM000673.1:g.118210529A>C	GRCh37
NC_000011.8:g.117715739A>C	NCBI36
NG_007566.1:g.471A>C , LRG_39:g.471A>C
NG_009891.1:g.7931T>G , LRG_37:g.7931T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695666.1:n.854T>G
ENST00000695667.1:n.372T>G
ENST00000695668.1:n.2352T>G
ENST00000300692.9:c.367T>G MANE Select	ENSP00000300692.4:p.Phe123Val
ENST00000300692.8:c.367T>G	ENSP00000300692.4:p.Phe123Val
ENST00000392884.2:c.275-320T>G	ENSP00000376622.2:n.275-320T>G
ENST00000526561.1:n.80-320T>G
ENST00000529594.5:c.148T>G	ENSP00000437335.1:p.Phe50Val
ENST00000534687.5:c.288-320T>G
NM_000732.4:c.367T>G , LRG_37t1:c.367T>G	NP_000723.1:p.Phe123Val
NM_001040651.1:c.275-320T>G	NP_001035741.1:n.275-320T>G
NM_001040651.2:c.275-320T>G	NP_001035741.1:n.275-320T>G
NM_000732.6:c.367T>G MANE Select	NP_000723.1:p.Phe123Val