Canonical Allele Identifier: CA382788228

Gene: CD3D

Linked Data

• MyVariant Identifiers: chr11:g.118210547G>C (hg19) ; chr11:g.118339832G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339832G>C , CM000673.2:g.118339832G>C	GRCh38
NC_000011.9:g.118210547G>C , CM000673.1:g.118210547G>C	GRCh37
NC_000011.8:g.117715757G>C	NCBI36
NG_007566.1:g.489G>C , LRG_39:g.489G>C
NG_009891.1:g.7913C>G , LRG_37:g.7913C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.836C>G
ENST00000695667.1:n.354C>G
ENST00000695668.1:n.2334C>G
ENST00000300692.9:c.349C>G MANE Select	ENSP00000300692.4:p.Leu117Val
ENST00000300692.8:c.349C>G	ENSP00000300692.4:p.Leu117Val
ENST00000392884.2:c.275-338C>G	ENSP00000376622.2:n.275-338C>G
ENST00000526561.1:n.80-338C>G
ENST00000529594.5:c.130C>G	ENSP00000437335.1:p.Leu44Val
ENST00000534687.5:c.288-338C>G
NM_000732.4:c.349C>G , LRG_37t1:c.349C>G	NP_000723.1:p.Leu117Val
NM_001040651.1:c.275-338C>G	NP_001035741.1:n.275-338C>G
NM_001040651.2:c.275-338C>G	NP_001035741.1:n.275-338C>G
NM_000732.6:c.349C>G MANE Select	NP_000723.1:p.Leu117Val