Canonical Allele Identifier: CA229522235

Gene: CD3D

Linked Data

• ClinVar Variation Id: 1291558
• ClinVar RCV Id: RCV001716866
• dbSNP Id: rs67065773
• gnomAD v2: 11-118210424-T-TACAC
• gnomAD v3: 11-118339709-T-TACAC
• gnomAD v4: 11-118339709-T-TACAC
• MyVariant Identifiers: chr11:g.118210457_118210458insCACA (hg19) ; chr11:g.118210428_118210429insACAC (hg19) ; chr11:g.118210424_118210425insACAC (hg19) ; chr11:g.118339742_118339743insCACA (hg38) ; chr11:g.118339713_118339714insACAC (hg38) ; chr11:g.118339709_118339710insACAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339739_118339742dup , CM000673.2:g.118339739_118339742dup	GRCh38
NC_000011.9:g.118210454_118210457dup , CM000673.1:g.118210454_118210457dup	GRCh37
NC_000011.8:g.117715664_117715667dup	NCBI36
NG_007566.1:g.396_399dup , LRG_39:g.396_399dup
NG_009891.1:g.8032_8035dup , LRG_37:g.8032_8035dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.955_958dup
ENST00000695667.1:n.473_476dup
ENST00000300692.9:c.406+62_406+65dup MANE Select	ENSP00000300692.4:n.406+62_406+65dup
ENST00000300692.8:c.406+62_406+65dup	ENSP00000300692.4:n.406+62_406+65dup
ENST00000392884.2:c.275-219_275-216dup	ENSP00000376622.2:n.275-219_275-216dup
ENST00000526561.1:n.80-219_80-216dup
ENST00000529594.5:c.187+62_187+65dup	ENSP00000437335.1:n.187+62_187+65dup
ENST00000534687.5:c.288-219_288-216dup
NM_000732.4:c.406+62_406+65dup , LRG_37t1:c.406+62_406+65dup	NP_000723.1:n.406+62_406+65dup
NM_001040651.1:c.275-219_275-216dup	NP_001035741.1:n.275-219_275-216dup
NM_001040651.2:c.275-219_275-216dup	NP_001035741.1:n.275-219_275-216dup
NM_000732.6:c.406+62_406+65dup MANE Select	NP_000723.1:n.406+62_406+65dup