Canonical Allele Identifier: CA382788055

Gene: CD3D

Linked Data

• MyVariant Identifiers: chr11:g.118210498A>G (hg19) ; chr11:g.118339783A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339783A>G , CM000673.2:g.118339783A>G	GRCh38
NC_000011.9:g.118210498A>G , CM000673.1:g.118210498A>G	GRCh37
NC_000011.8:g.117715708A>G	NCBI36
NG_007566.1:g.440A>G , LRG_39:g.440A>G
NG_009891.1:g.7962T>C , LRG_37:g.7962T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.885T>C
ENST00000695667.1:n.403T>C
ENST00000695668.1:n.2383T>C
ENST00000300692.9:c.398T>C MANE Select	ENSP00000300692.4:p.Leu133Pro
ENST00000300692.8:c.398T>C	ENSP00000300692.4:p.Leu133Pro
ENST00000392884.2:c.275-289T>C	ENSP00000376622.2:n.275-289T>C
ENST00000526561.1:n.80-289T>C
ENST00000529594.5:c.179T>C	ENSP00000437335.1:p.Leu60Pro
ENST00000534687.5:c.288-289T>C
NM_000732.4:c.398T>C , LRG_37t1:c.398T>C	NP_000723.1:p.Leu133Pro
NM_001040651.1:c.275-289T>C	NP_001035741.1:n.275-289T>C
NM_001040651.2:c.275-289T>C	NP_001035741.1:n.275-289T>C
NM_000732.6:c.398T>C MANE Select	NP_000723.1:p.Leu133Pro