Canonical Allele Identifier: CA2725025437

Gene: CD3D

Linked Data

• dbSNP Id: rs2134059075

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339714_118339715insAACA , CM000673.2:g.118339714_118339715insAACA	GRCh38
NC_000011.9:g.118210429_118210430insAACA , CM000673.1:g.118210429_118210430insAACA	GRCh37
NC_000011.8:g.117715639_117715640insAACA	NCBI36
NG_007566.1:g.371_372insAACA , LRG_39:g.371_372insAACA
NG_009891.1:g.8033_8034insTTGT , LRG_37:g.8033_8034insTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.956_957insTTGT
ENST00000695667.1:n.474_475insTTGT
ENST00000300692.9:c.406+63_406+64insTTGT MANE Select	ENSP00000300692.4:n.406+63_406+64insTTGT
ENST00000300692.8:c.406+63_406+64insTTGT	ENSP00000300692.4:n.406+63_406+64insTTGT
ENST00000392884.2:c.275-218_275-217insTTGT	ENSP00000376622.2:n.275-218_275-217insTTGT
ENST00000526561.1:n.80-218_80-217insTTGT
ENST00000529594.5:c.187+63_187+64insTTGT	ENSP00000437335.1:n.187+63_187+64insTTGT
ENST00000534687.5:c.288-218_288-217insTTGT
NM_000732.4:c.406+63_406+64insTTGT , LRG_37t1:c.406+63_406+64insTTGT	NP_000723.1:n.406+63_406+64insTTGT
NM_001040651.1:c.275-218_275-217insTTGT	NP_001035741.1:n.275-218_275-217insTTGT
NM_001040651.2:c.275-218_275-217insTTGT	NP_001035741.1:n.275-218_275-217insTTGT
NM_000732.6:c.406+63_406+64insTTGT MANE Select	NP_000723.1:n.406+63_406+64insTTGT