Canonical Allele Identifier: CA477087304

Gene: CD3D

Linked Data

• MyVariant Identifiers: chr11:g.118210578G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339863G>T , CM000673.2:g.118339863G>T	GRCh38
NC_000011.9:g.118210578G>T , CM000673.1:g.118210578G>T	GRCh37
NC_000011.8:g.117715788G>T	NCBI36
NG_007566.1:g.520G>T , LRG_39:g.520G>T
NG_009891.1:g.7882C>A , LRG_37:g.7882C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.805C>A
ENST00000695667.1:n.323C>A
ENST00000695668.1:n.2303C>A
ENST00000300692.9:c.318C>A MANE Select	ENSP00000300692.4:p.Gly106=
ENST00000300692.8:c.318C>A	ENSP00000300692.4:p.Gly106=
ENST00000392884.2:c.275-369C>A	ENSP00000376622.2:n.275-369C>A
ENST00000526561.1:n.80-369C>A
ENST00000529594.5:c.99C>A	ENSP00000437335.1:p.Gly33=
ENST00000534687.5:c.288-369C>A
NM_000732.4:c.318C>A , LRG_37t1:c.318C>A	NP_000723.1:p.Gly106=
NM_001040651.1:c.275-369C>A	NP_001035741.1:n.275-369C>A
NM_001040651.2:c.275-369C>A	NP_001035741.1:n.275-369C>A
NM_000732.6:c.318C>A MANE Select	NP_000723.1:p.Gly106=