Canonical Allele Identifier: CA382788080

Gene: CD3D

Linked Data

• MyVariant Identifiers: chr11:g.118210505C>T (hg19) ; chr11:g.118339790C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339790C>T , CM000673.2:g.118339790C>T	GRCh38
NC_000011.9:g.118210505C>T , CM000673.1:g.118210505C>T	GRCh37
NC_000011.8:g.117715715C>T	NCBI36
NG_007566.1:g.447C>T , LRG_39:g.447C>T
NG_009891.1:g.7955G>A , LRG_37:g.7955G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.878G>A
ENST00000695667.1:n.396G>A
ENST00000695668.1:n.2376G>A
ENST00000300692.9:c.391G>A MANE Select	ENSP00000300692.4:p.Gly131Arg
ENST00000300692.8:c.391G>A	ENSP00000300692.4:p.Gly131Arg
ENST00000392884.2:c.275-296G>A	ENSP00000376622.2:n.275-296G>A
ENST00000526561.1:n.80-296G>A
ENST00000529594.5:c.172G>A	ENSP00000437335.1:p.Gly58Arg
ENST00000534687.5:c.288-296G>A
NM_000732.4:c.391G>A , LRG_37t1:c.391G>A	NP_000723.1:p.Gly131Arg
NM_001040651.1:c.275-296G>A	NP_001035741.1:n.275-296G>A
NM_001040651.2:c.275-296G>A	NP_001035741.1:n.275-296G>A
NM_000732.6:c.391G>A MANE Select	NP_000723.1:p.Gly131Arg