Canonical Allele Identifier: CA2616232513

Gene: CD3D

Linked Data

• gnomAD v4: 11-118340037-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118340037C>A , CM000673.2:g.118340037C>A	GRCh38
NC_000011.9:g.118210752C>A , CM000673.1:g.118210752C>A	GRCh37
NC_000011.8:g.117715962C>A	NCBI36
NG_007566.1:g.694C>A , LRG_39:g.694C>A
NG_009891.1:g.7708G>T , LRG_37:g.7708G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.631G>T
ENST00000695667.1:n.280-131G>T
ENST00000695668.1:n.2260-131G>T
ENST00000300692.9:c.275-131G>T MANE Select	ENSP00000300692.4:n.275-131G>T
ENST00000300692.8:c.275-131G>T	ENSP00000300692.4:n.275-131G>T
ENST00000392884.2:c.274+338G>T	ENSP00000376622.2:n.274+338G>T
ENST00000526561.1:n.80-543G>T
ENST00000529594.5:c.56-131G>T	ENSP00000437335.1:n.56-131G>T
ENST00000534687.5:c.287+338G>T
NM_000732.4:c.275-131G>T , LRG_37t1:c.275-131G>T	NP_000723.1:n.275-131G>T
NM_001040651.1:c.274+338G>T	NP_001035741.1:n.274+338G>T
NM_001040651.2:c.274+338G>T	NP_001035741.1:n.274+338G>T
NM_000732.6:c.275-131G>T MANE Select	NP_000723.1:n.275-131G>T