Canonical Allele Identifier: CA382788380

Gene: CD3D

Linked Data

• MyVariant Identifiers: chr11:g.118210594G>C (hg19) ; chr11:g.118339879G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339879G>C , CM000673.2:g.118339879G>C	GRCh38
NC_000011.9:g.118210594G>C , CM000673.1:g.118210594G>C	GRCh37
NC_000011.8:g.117715804G>C	NCBI36
NG_007566.1:g.536G>C , LRG_39:g.536G>C
NG_009891.1:g.7866C>G , LRG_37:g.7866C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.789C>G
ENST00000695667.1:n.307C>G
ENST00000695668.1:n.2287C>G
ENST00000300692.9:c.302C>G MANE Select	ENSP00000300692.4:p.Pro101Arg
ENST00000300692.8:c.302C>G	ENSP00000300692.4:p.Pro101Arg
ENST00000392884.2:c.275-385C>G	ENSP00000376622.2:n.275-385C>G
ENST00000526561.1:n.80-385C>G
ENST00000529594.5:c.83C>G	ENSP00000437335.1:p.Pro28Arg
ENST00000534687.5:c.288-385C>G
NM_000732.4:c.302C>G , LRG_37t1:c.302C>G	NP_000723.1:p.Pro101Arg
NM_001040651.1:c.275-385C>G	NP_001035741.1:n.275-385C>G
NM_001040651.2:c.275-385C>G	NP_001035741.1:n.275-385C>G
NM_000732.6:c.302C>G MANE Select	NP_000723.1:p.Pro101Arg