Canonical Allele Identifier: CA2003456960

Gene: CD3D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339713C= , CM000673.2:g.118339713C=	GRCh38
NC_000011.9:g.118210428C= , CM000673.1:g.118210428C=	GRCh37
NC_000011.8:g.117715638C=	NCBI36
NG_007566.1:g.370C= , LRG_39:g.370C=
NG_009891.1:g.8032G= , LRG_37:g.8032G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.955G=
ENST00000695667.1:n.473G=
ENST00000300692.9:c.406+62G= MANE Select	ENSP00000300692.4:n.406+62G=
ENST00000300692.8:c.406+62G=	ENSP00000300692.4:n.406+62G=
ENST00000392884.2:c.275-219G=	ENSP00000376622.2:n.275-219G=
ENST00000526561.1:n.80-219G=
ENST00000529594.5:c.187+62G=	ENSP00000437335.1:n.187+62G=
ENST00000534687.5:c.288-219G=
NM_000732.4:c.406+62G= , LRG_37t1:c.406+62G=	NP_000723.1:n.406+62G=
NM_001040651.1:c.275-219G=	NP_001035741.1:n.275-219G=
NM_001040651.2:c.275-219G=	NP_001035741.1:n.275-219G=
NM_000732.6:c.406+62G= MANE Select	NP_000723.1:n.406+62G=