Canonical Allele Identifier: CA2724964677

Gene: CD3D

Linked Data

• dbSNP Id: rs1267632571

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339718_118339719insAACA , CM000673.2:g.118339718_118339719insAACA	GRCh38
NC_000011.9:g.118210433_118210434insAACA , CM000673.1:g.118210433_118210434insAACA	GRCh37
NC_000011.8:g.117715643_117715644insAACA	NCBI36
NG_007566.1:g.375_376insAACA , LRG_39:g.375_376insAACA
NG_009891.1:g.8029_8030insTTGT , LRG_37:g.8029_8030insTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.952_953insTTGT
ENST00000695667.1:n.470_471insTTGT
ENST00000300692.9:c.406+59_406+60insTTGT MANE Select	ENSP00000300692.4:n.406+59_406+60insTTGT
ENST00000300692.8:c.406+59_406+60insTTGT	ENSP00000300692.4:n.406+59_406+60insTTGT
ENST00000392884.2:c.275-222_275-221insTTGT	ENSP00000376622.2:n.275-222_275-221insTTGT
ENST00000526561.1:n.80-222_80-221insTTGT
ENST00000529594.5:c.187+59_187+60insTTGT	ENSP00000437335.1:n.187+59_187+60insTTGT
ENST00000534687.5:c.288-222_288-221insTTGT
NM_000732.4:c.406+59_406+60insTTGT , LRG_37t1:c.406+59_406+60insTTGT	NP_000723.1:n.406+59_406+60insTTGT
NM_001040651.1:c.275-222_275-221insTTGT	NP_001035741.1:n.275-222_275-221insTTGT
NM_001040651.2:c.275-222_275-221insTTGT	NP_001035741.1:n.275-222_275-221insTTGT
NM_000732.6:c.406+59_406+60insTTGT MANE Select	NP_000723.1:n.406+59_406+60insTTGT