Canonical Allele Identifier: CA477087327

Gene: CD3D

Linked Data

• ClinVar Variation Id: 2839166
• ClinVar RCV Id: RCV003744414
• MyVariant Identifiers: chr11:g.118210596A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339881A>G , CM000673.2:g.118339881A>G	GRCh38
NC_000011.9:g.118210596A>G , CM000673.1:g.118210596A>G	GRCh37
NC_000011.8:g.117715806A>G	NCBI36
NG_007566.1:g.538A>G , LRG_39:g.538A>G
NG_009891.1:g.7864T>C , LRG_37:g.7864T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.787T>C
ENST00000695667.1:n.305T>C
ENST00000695668.1:n.2285T>C
ENST00000300692.9:c.300T>C MANE Select	ENSP00000300692.4:p.Asp100=
ENST00000300692.8:c.300T>C	ENSP00000300692.4:p.Asp100=
ENST00000392884.2:c.275-387T>C	ENSP00000376622.2:n.275-387T>C
ENST00000526561.1:n.80-387T>C
ENST00000529594.5:c.81T>C	ENSP00000437335.1:p.Asp27=
ENST00000534687.5:c.288-387T>C
NM_000732.4:c.300T>C , LRG_37t1:c.300T>C	NP_000723.1:p.Asp100=
NM_001040651.1:c.275-387T>C	NP_001035741.1:n.275-387T>C
NM_001040651.2:c.275-387T>C	NP_001035741.1:n.275-387T>C
NM_000732.6:c.300T>C MANE Select	NP_000723.1:p.Asp100=