Canonical Allele Identifier: CA477087322

Gene: CD3D

Linked Data

• ClinVar Variation Id: 2824653
• ClinVar RCV Id: RCV003744225
• MyVariant Identifiers: chr11:g.118210593T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339878T>C , CM000673.2:g.118339878T>C	GRCh38
NC_000011.9:g.118210593T>C , CM000673.1:g.118210593T>C	GRCh37
NC_000011.8:g.117715803T>C	NCBI36
NG_007566.1:g.535T>C , LRG_39:g.535T>C
NG_009891.1:g.7867A>G , LRG_37:g.7867A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.790A>G
ENST00000695667.1:n.308A>G
ENST00000695668.1:n.2288A>G
ENST00000300692.9:c.303A>G MANE Select	ENSP00000300692.4:p.Pro101=
ENST00000300692.8:c.303A>G	ENSP00000300692.4:p.Pro101=
ENST00000392884.2:c.275-384A>G	ENSP00000376622.2:n.275-384A>G
ENST00000526561.1:n.80-384A>G
ENST00000529594.5:c.84A>G	ENSP00000437335.1:p.Pro28=
ENST00000534687.5:c.288-384A>G
NM_000732.4:c.303A>G , LRG_37t1:c.303A>G	NP_000723.1:p.Pro101=
NM_001040651.1:c.275-384A>G	NP_001035741.1:n.275-384A>G
NM_001040651.2:c.275-384A>G	NP_001035741.1:n.275-384A>G
NM_000732.6:c.303A>G MANE Select	NP_000723.1:p.Pro101=