Canonical Allele Identifier: CA477087055

Gene: CD3D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339213T>G , CM000673.2:g.118339213T>G	GRCh38
NC_000011.9:g.118209928T>G , CM000673.1:g.118209928T>G	GRCh37
NC_000011.8:g.117715138T>G	NCBI36
NG_009891.1:g.8532A>C , LRG_37:g.8532A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000732.6:c.465A>C MANE Select	NP_000723.1:p.Arg155=
ENST00000300692.9:c.465A>C MANE Select	ENSP00000300692.4:p.Arg155=
NM_000732.4:c.465A>C , LRG_37t1:c.465A>C	NP_000723.1:p.Arg155=
NM_001040651.1:c.333A>C	NP_001035741.1:p.Arg111=
NM_001040651.2:c.333A>C	NP_001035741.1:p.Arg111=
ENST00000300692.8:c.465A>C	ENSP00000300692.4:p.Arg155=
ENST00000392884.2:c.333A>C	ENSP00000376622.2:p.Arg111=
ENST00000526561.1:n.138A>C
ENST00000529594.5:c.246A>C	ENSP00000437335.1:p.Arg82=
ENST00000534687.5:c.346A>C
ENST00000695666.1:n.1232A>C
ENST00000695667.1:n.750A>C