Canonical Allele Identifier: CA477087213

Gene: CD3D

Linked Data

• MyVariant Identifiers: chr11:g.118210518A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339803A>T , CM000673.2:g.118339803A>T	GRCh38
NC_000011.9:g.118210518A>T , CM000673.1:g.118210518A>T	GRCh37
NC_000011.8:g.117715728A>T	NCBI36
NG_007566.1:g.460A>T , LRG_39:g.460A>T
NG_009891.1:g.7942T>A , LRG_37:g.7942T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695666.1:n.865T>A
ENST00000695667.1:n.383T>A
ENST00000695668.1:n.2363T>A
ENST00000300692.9:c.378T>A MANE Select	ENSP00000300692.4:p.Ala126=
ENST00000300692.8:c.378T>A	ENSP00000300692.4:p.Ala126=
ENST00000392884.2:c.275-309T>A	ENSP00000376622.2:n.275-309T>A
ENST00000526561.1:n.80-309T>A
ENST00000529594.5:c.159T>A	ENSP00000437335.1:p.Ala53=
ENST00000534687.5:c.288-309T>A
NM_000732.4:c.378T>A , LRG_37t1:c.378T>A	NP_000723.1:p.Ala126=
NM_001040651.1:c.275-309T>A	NP_001035741.1:n.275-309T>A
NM_001040651.2:c.275-309T>A	NP_001035741.1:n.275-309T>A
NM_000732.6:c.378T>A MANE Select	NP_000723.1:p.Ala126=