Canonical Allele Identifier: CA382788451

Gene: CD3D

Linked Data

• MyVariant Identifiers: chr11:g.118210610A>G (hg19) ; chr11:g.118339895A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339895A>G , CM000673.2:g.118339895A>G	GRCh38
NC_000011.9:g.118210610A>G , CM000673.1:g.118210610A>G	GRCh37
NC_000011.8:g.117715820A>G	NCBI36
NG_007566.1:g.552A>G , LRG_39:g.552A>G
NG_009891.1:g.7850T>C , LRG_37:g.7850T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.773T>C
ENST00000695667.1:n.291T>C
ENST00000695668.1:n.2271T>C
ENST00000300692.9:c.286T>C MANE Select	ENSP00000300692.4:p.Cys96Arg
ENST00000300692.8:c.286T>C	ENSP00000300692.4:p.Cys96Arg
ENST00000392884.2:c.275-401T>C	ENSP00000376622.2:n.275-401T>C
ENST00000526561.1:n.80-401T>C
ENST00000529594.5:c.67T>C	ENSP00000437335.1:p.Cys23Arg
ENST00000534687.5:c.288-401T>C
NM_000732.4:c.286T>C , LRG_37t1:c.286T>C	NP_000723.1:p.Cys96Arg
NM_001040651.1:c.275-401T>C	NP_001035741.1:n.275-401T>C
NM_001040651.2:c.275-401T>C	NP_001035741.1:n.275-401T>C
NM_000732.6:c.286T>C MANE Select	NP_000723.1:p.Cys96Arg