Canonical Allele Identifier: CA2616232466

Gene: CD3D

Linked Data

• gnomAD v4: 11-118339969-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339969G>T , CM000673.2:g.118339969G>T	GRCh38
NC_000011.9:g.118210684G>T , CM000673.1:g.118210684G>T	GRCh37
NC_000011.8:g.117715894G>T	NCBI36
NG_007566.1:g.626G>T , LRG_39:g.626G>T
NG_009891.1:g.7776C>A , LRG_37:g.7776C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.699C>A
ENST00000695667.1:n.280-63C>A
ENST00000695668.1:n.2260-63C>A
ENST00000300692.9:c.275-63C>A MANE Select	ENSP00000300692.4:n.275-63C>A
ENST00000300692.8:c.275-63C>A	ENSP00000300692.4:n.275-63C>A
ENST00000392884.2:c.274+406C>A	ENSP00000376622.2:n.274+406C>A
ENST00000526561.1:n.80-475C>A
ENST00000529594.5:c.56-63C>A	ENSP00000437335.1:n.56-63C>A
ENST00000534687.5:c.287+406C>A
NM_000732.4:c.275-63C>A , LRG_37t1:c.275-63C>A	NP_000723.1:n.275-63C>A
NM_001040651.1:c.274+406C>A	NP_001035741.1:n.274+406C>A
NM_001040651.2:c.274+406C>A	NP_001035741.1:n.274+406C>A
NM_000732.6:c.275-63C>A MANE Select	NP_000723.1:n.275-63C>A