Canonical Allele Identifier: CA382788414

Gene: CD3D

Linked Data

• MyVariant Identifiers: chr11:g.118210601G>T (hg19) ; chr11:g.118339886G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339886G>T , CM000673.2:g.118339886G>T	GRCh38
NC_000011.9:g.118210601G>T , CM000673.1:g.118210601G>T	GRCh37
NC_000011.8:g.117715811G>T	NCBI36
NG_007566.1:g.543G>T , LRG_39:g.543G>T
NG_009891.1:g.7859C>A , LRG_37:g.7859C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.782C>A
ENST00000695667.1:n.300C>A
ENST00000695668.1:n.2280C>A
ENST00000300692.9:c.295C>A MANE Select	ENSP00000300692.4:p.Leu99Met
ENST00000300692.8:c.295C>A	ENSP00000300692.4:p.Leu99Met
ENST00000392884.2:c.275-392C>A	ENSP00000376622.2:n.275-392C>A
ENST00000526561.1:n.80-392C>A
ENST00000529594.5:c.76C>A	ENSP00000437335.1:p.Leu26Met
ENST00000534687.5:c.288-392C>A
NM_000732.4:c.295C>A , LRG_37t1:c.295C>A	NP_000723.1:p.Leu99Met
NM_001040651.1:c.275-392C>A	NP_001035741.1:n.275-392C>A
NM_001040651.2:c.275-392C>A	NP_001035741.1:n.275-392C>A
NM_000732.6:c.295C>A MANE Select	NP_000723.1:p.Leu99Met