Canonical Allele Identifier: CA477087350

Gene: CD3D

Linked Data

• MyVariant Identifiers: chr11:g.118210617G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339902G>A , CM000673.2:g.118339902G>A	GRCh38
NC_000011.9:g.118210617G>A , CM000673.1:g.118210617G>A	GRCh37
NC_000011.8:g.117715827G>A	NCBI36
NG_007566.1:g.559G>A , LRG_39:g.559G>A
NG_009891.1:g.7843C>T , LRG_37:g.7843C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.766C>T
ENST00000695667.1:n.284C>T
ENST00000695668.1:n.2264C>T
ENST00000300692.9:c.279C>T MANE Select	ENSP00000300692.4:p.Cys93=
ENST00000300692.8:c.279C>T	ENSP00000300692.4:p.Cys93=
ENST00000392884.2:c.275-408C>T	ENSP00000376622.2:n.275-408C>T
ENST00000526561.1:n.80-408C>T
ENST00000529594.5:c.60C>T	ENSP00000437335.1:p.Cys20=
ENST00000534687.5:c.288-408C>T
NM_000732.4:c.279C>T , LRG_37t1:c.279C>T	NP_000723.1:p.Cys93=
NM_001040651.1:c.275-408C>T	NP_001035741.1:n.275-408C>T
NM_001040651.2:c.275-408C>T	NP_001035741.1:n.275-408C>T
NM_000732.6:c.279C>T MANE Select	NP_000723.1:p.Cys93=