Canonical Allele Identifier: CA382788087

Gene: CD3D

Linked Data

• MyVariant Identifiers: chr11:g.118210508T>A (hg19) ; chr11:g.118339793T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339793T>A , CM000673.2:g.118339793T>A	GRCh38
NC_000011.9:g.118210508T>A , CM000673.1:g.118210508T>A	GRCh37
NC_000011.8:g.117715718T>A	NCBI36
NG_007566.1:g.450T>A , LRG_39:g.450T>A
NG_009891.1:g.7952A>T , LRG_37:g.7952A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.875A>T
ENST00000695667.1:n.393A>T
ENST00000695668.1:n.2373A>T
ENST00000300692.9:c.388A>T MANE Select	ENSP00000300692.4:p.Thr130Ser
ENST00000300692.8:c.388A>T	ENSP00000300692.4:p.Thr130Ser
ENST00000392884.2:c.275-299A>T	ENSP00000376622.2:n.275-299A>T
ENST00000526561.1:n.80-299A>T
ENST00000529594.5:c.169A>T	ENSP00000437335.1:p.Thr57Ser
ENST00000534687.5:c.288-299A>T
NM_000732.4:c.388A>T , LRG_37t1:c.388A>T	NP_000723.1:p.Thr130Ser
NM_001040651.1:c.275-299A>T	NP_001035741.1:n.275-299A>T
NM_001040651.2:c.275-299A>T	NP_001035741.1:n.275-299A>T
NM_000732.6:c.388A>T MANE Select	NP_000723.1:p.Thr130Ser