Canonical Allele Identifier: CA382788447

Gene: CD3D

Linked Data

• gnomAD v4: 11-118339894-C-T
• MyVariant Identifiers: chr11:g.118210609C>T (hg19) ; chr11:g.118339894C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339894C>T , CM000673.2:g.118339894C>T	GRCh38
NC_000011.9:g.118210609C>T , CM000673.1:g.118210609C>T	GRCh37
NC_000011.8:g.117715819C>T	NCBI36
NG_007566.1:g.551C>T , LRG_39:g.551C>T
NG_009891.1:g.7851G>A , LRG_37:g.7851G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.774G>A
ENST00000695667.1:n.292G>A
ENST00000695668.1:n.2272G>A
ENST00000300692.9:c.287G>A MANE Select	ENSP00000300692.4:p.Cys96Tyr
ENST00000300692.8:c.287G>A	ENSP00000300692.4:p.Cys96Tyr
ENST00000392884.2:c.275-400G>A	ENSP00000376622.2:n.275-400G>A
ENST00000526561.1:n.80-400G>A
ENST00000529594.5:c.68G>A	ENSP00000437335.1:p.Cys23Tyr
ENST00000534687.5:c.288-400G>A
NM_000732.4:c.287G>A , LRG_37t1:c.287G>A	NP_000723.1:p.Cys96Tyr
NM_001040651.1:c.275-400G>A	NP_001035741.1:n.275-400G>A
NM_001040651.2:c.275-400G>A	NP_001035741.1:n.275-400G>A
NM_000732.6:c.287G>A MANE Select	NP_000723.1:p.Cys96Tyr