Canonical Allele Identifier: CA382788142

Gene: CD3D

Linked Data

• MyVariant Identifiers: chr11:g.118210523A>T (hg19) ; chr11:g.118339808A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339808A>T , CM000673.2:g.118339808A>T	GRCh38
NC_000011.9:g.118210523A>T , CM000673.1:g.118210523A>T	GRCh37
NC_000011.8:g.117715733A>T	NCBI36
NG_007566.1:g.465A>T , LRG_39:g.465A>T
NG_009891.1:g.7937T>A , LRG_37:g.7937T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695666.1:n.860T>A
ENST00000695667.1:n.378T>A
ENST00000695668.1:n.2358T>A
ENST00000300692.9:c.373T>A MANE Select	ENSP00000300692.4:p.Phe125Ile
ENST00000300692.8:c.373T>A	ENSP00000300692.4:p.Phe125Ile
ENST00000392884.2:c.275-314T>A	ENSP00000376622.2:n.275-314T>A
ENST00000526561.1:n.80-314T>A
ENST00000529594.5:c.154T>A	ENSP00000437335.1:p.Phe52Ile
ENST00000534687.5:c.288-314T>A
NM_000732.4:c.373T>A , LRG_37t1:c.373T>A	NP_000723.1:p.Phe125Ile
NM_001040651.1:c.275-314T>A	NP_001035741.1:n.275-314T>A
NM_001040651.2:c.275-314T>A	NP_001035741.1:n.275-314T>A
NM_000732.6:c.373T>A MANE Select	NP_000723.1:p.Phe125Ile