Canonical Allele Identifier: CA477087200

Gene: CD3D

Linked Data

• MyVariant Identifiers: chr11:g.118210502T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339787T>G , CM000673.2:g.118339787T>G	GRCh38
NC_000011.9:g.118210502T>G , CM000673.1:g.118210502T>G	GRCh37
NC_000011.8:g.117715712T>G	NCBI36
NG_007566.1:g.444T>G , LRG_39:g.444T>G
NG_009891.1:g.7958A>C , LRG_37:g.7958A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.881A>C
ENST00000695667.1:n.399A>C
ENST00000695668.1:n.2379A>C
ENST00000300692.9:c.394A>C MANE Select	ENSP00000300692.4:p.Arg132=
ENST00000300692.8:c.394A>C	ENSP00000300692.4:p.Arg132=
ENST00000392884.2:c.275-293A>C	ENSP00000376622.2:n.275-293A>C
ENST00000526561.1:n.80-293A>C
ENST00000529594.5:c.175A>C	ENSP00000437335.1:p.Arg59=
ENST00000534687.5:c.288-293A>C
NM_000732.4:c.394A>C , LRG_37t1:c.394A>C	NP_000723.1:p.Arg132=
NM_001040651.1:c.275-293A>C	NP_001035741.1:n.275-293A>C
NM_001040651.2:c.275-293A>C	NP_001035741.1:n.275-293A>C
NM_000732.6:c.394A>C MANE Select	NP_000723.1:p.Arg132=