Canonical Allele Identifier: CA477087199

Gene: CD3D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339785C>T , CM000673.2:g.118339785C>T	GRCh38
NC_000011.9:g.118210500C>T , CM000673.1:g.118210500C>T	GRCh37
NC_000011.8:g.117715710C>T	NCBI36
NG_007566.1:g.442C>T , LRG_39:g.442C>T
NG_009891.1:g.7960G>A , LRG_37:g.7960G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000732.6:c.396G>A MANE Select	NP_000723.1:p.Arg132=
ENST00000300692.9:c.396G>A MANE Select	ENSP00000300692.4:p.Arg132=
NM_000732.4:c.396G>A , LRG_37t1:c.396G>A	NP_000723.1:p.Arg132=
NM_001040651.1:c.275-291G>A	NP_001035741.1:n.275-291G>A
NM_001040651.2:c.275-291G>A	NP_001035741.1:n.275-291G>A
ENST00000300692.8:c.396G>A	ENSP00000300692.4:p.Arg132=
ENST00000392884.2:c.275-291G>A	ENSP00000376622.2:n.275-291G>A
ENST00000526561.1:n.80-291G>A
ENST00000529594.5:c.177G>A	ENSP00000437335.1:p.Arg59=
ENST00000534687.5:c.288-291G>A
ENST00000695666.1:n.883G>A
ENST00000695667.1:n.401G>A
ENST00000695668.1:n.2381G>A