Canonical Allele Identifier: CA382788000

Gene: CD3D

Linked Data

• MyVariant Identifiers: chr11:g.118210456_118210457insCA (hg19) ; chr11:g.118339741_118339742insCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339741_118339742insCA , CM000673.2:g.118339741_118339742insCA	GRCh38
NC_000011.9:g.118210456_118210457insCA , CM000673.1:g.118210456_118210457insCA	GRCh37
NC_000011.8:g.117715666_117715667insCA	NCBI36
NG_007566.1:g.398_399insCA , LRG_39:g.398_399insCA
NG_009891.1:g.8003_8004insTG , LRG_37:g.8003_8004insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.926_927insTG
ENST00000695667.1:n.444_445insTG
ENST00000695668.1:n.2424_2425insTG
ENST00000300692.9:c.406+33_406+34insTG MANE Select	ENSP00000300692.4:n.406+33_406+34insTG
ENST00000300692.8:c.406+33_406+34insTG	ENSP00000300692.4:n.406+33_406+34insTG
ENST00000392884.2:c.275-248_275-247insTG	ENSP00000376622.2:n.275-248_275-247insTG
ENST00000526561.1:n.80-248_80-247insTG
ENST00000529594.5:c.187+33_187+34insTG	ENSP00000437335.1:n.187+33_187+34insTG
ENST00000534687.5:c.288-248_288-247insTG
NM_000732.4:c.406+33_406+34insTG , LRG_37t1:c.406+33_406+34insTG	NP_000723.1:n.406+33_406+34insTG
NM_001040651.1:c.275-248_275-247insTG	NP_001035741.1:n.275-248_275-247insTG
NM_001040651.2:c.275-248_275-247insTG	NP_001035741.1:n.275-248_275-247insTG
NM_000732.6:c.406+33_406+34insTG MANE Select	NP_000723.1:n.406+33_406+34insTG