Canonical Allele Identifier: CA2616232459

Gene: CD3D

Linked Data

• gnomAD v4: 11-118339958-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339958A>T , CM000673.2:g.118339958A>T	GRCh38
NC_000011.9:g.118210673A>T , CM000673.1:g.118210673A>T	GRCh37
NC_000011.8:g.117715883A>T	NCBI36
NG_007566.1:g.615A>T , LRG_39:g.615A>T
NG_009891.1:g.7787T>A , LRG_37:g.7787T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.710T>A
ENST00000695667.1:n.280-52T>A
ENST00000695668.1:n.2260-52T>A
ENST00000300692.9:c.275-52T>A MANE Select	ENSP00000300692.4:n.275-52T>A
ENST00000300692.8:c.275-52T>A	ENSP00000300692.4:n.275-52T>A
ENST00000392884.2:c.274+417T>A	ENSP00000376622.2:n.274+417T>A
ENST00000526561.1:n.80-464T>A
ENST00000529594.5:c.56-52T>A	ENSP00000437335.1:n.56-52T>A
ENST00000534687.5:c.287+417T>A
NM_000732.4:c.275-52T>A , LRG_37t1:c.275-52T>A	NP_000723.1:n.275-52T>A
NM_001040651.1:c.274+417T>A	NP_001035741.1:n.274+417T>A
NM_001040651.2:c.274+417T>A	NP_001035741.1:n.274+417T>A
NM_000732.6:c.275-52T>A MANE Select	NP_000723.1:n.275-52T>A