Canonical Allele Identifier: CA477087341

Gene: CD3D

Linked Data

• MyVariant Identifiers: chr11:g.118210605C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339890C>A , CM000673.2:g.118339890C>A	GRCh38
NC_000011.9:g.118210605C>A , CM000673.1:g.118210605C>A	GRCh37
NC_000011.8:g.117715815C>A	NCBI36
NG_007566.1:g.547C>A , LRG_39:g.547C>A
NG_009891.1:g.7855G>T , LRG_37:g.7855G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.778G>T
ENST00000695667.1:n.296G>T
ENST00000695668.1:n.2276G>T
ENST00000300692.9:c.291G>T MANE Select	ENSP00000300692.4:p.Val97=
ENST00000300692.8:c.291G>T	ENSP00000300692.4:p.Val97=
ENST00000392884.2:c.275-396G>T	ENSP00000376622.2:n.275-396G>T
ENST00000526561.1:n.80-396G>T
ENST00000529594.5:c.72G>T	ENSP00000437335.1:p.Val24=
ENST00000534687.5:c.288-396G>T
NM_000732.4:c.291G>T , LRG_37t1:c.291G>T	NP_000723.1:p.Val97=
NM_001040651.1:c.275-396G>T	NP_001035741.1:n.275-396G>T
NM_001040651.2:c.275-396G>T	NP_001035741.1:n.275-396G>T
NM_000732.6:c.291G>T MANE Select	NP_000723.1:p.Val97=