Canonical Allele Identifier: CA2003456969

Gene: CD3D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339723C= , CM000673.2:g.118339723C=	GRCh38
NC_000011.9:g.118210438C= , CM000673.1:g.118210438C=	GRCh37
NC_000011.8:g.117715648C=	NCBI36
NG_007566.1:g.380C= , LRG_39:g.380C=
NG_009891.1:g.8022G= , LRG_37:g.8022G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.945G=
ENST00000695667.1:n.463G=
ENST00000695668.1:n.2443G=
ENST00000300692.9:c.406+52G= MANE Select	ENSP00000300692.4:n.406+52G=
ENST00000300692.8:c.406+52G=	ENSP00000300692.4:n.406+52G=
ENST00000392884.2:c.275-229G=	ENSP00000376622.2:n.275-229G=
ENST00000526561.1:n.80-229G=
ENST00000529594.5:c.187+52G=	ENSP00000437335.1:n.187+52G=
ENST00000534687.5:c.288-229G=
NM_000732.4:c.406+52G= , LRG_37t1:c.406+52G=	NP_000723.1:n.406+52G=
NM_001040651.1:c.275-229G=	NP_001035741.1:n.275-229G=
NM_001040651.2:c.275-229G=	NP_001035741.1:n.275-229G=
NM_000732.6:c.406+52G= MANE Select	NP_000723.1:n.406+52G=