Canonical Allele Identifier: CA2003456940
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339692G= , CM000673.2:g.118339692G= GRCh38
NC_000011.9:g.118210407G= , CM000673.1:g.118210407G= GRCh37
NC_000011.8:g.117715617G= NCBI36
NG_007566.1:g.349G= , LRG_39:g.349G=
NG_009891.1:g.8053C= , LRG_37:g.8053C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.976C=
ENST00000695667.1:n.494C=
ENST00000300692.9:c.406+83C= MANE Select ENSP00000300692.4:n.406+83C=
ENST00000300692.8:c.406+83C= ENSP00000300692.4:n.406+83C=
ENST00000392884.2:c.275-198C= ENSP00000376622.2:n.275-198C=
ENST00000526561.1:n.80-198C=
ENST00000529594.5:c.187+83C= ENSP00000437335.1:n.187+83C=
ENST00000534687.5:c.288-198C=
NM_000732.4:c.406+83C= , LRG_37t1:c.406+83C= NP_000723.1:n.406+83C=
NM_001040651.1:c.275-198C= NP_001035741.1:n.275-198C=
NM_001040651.2:c.275-198C= NP_001035741.1:n.275-198C=
NM_000732.6:c.406+83C= MANE Select NP_000723.1:n.406+83C=