Canonical Allele Identifier: CA2003456949

Gene: CD3D

Linked Data

• dbSNP Id: rs1948281729

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339709_118339710del , CM000673.2:g.118339709_118339710del	GRCh38
NC_000011.9:g.118210424_118210425del , CM000673.1:g.118210424_118210425del	GRCh37
NC_000011.8:g.117715634_117715635del	NCBI36
NG_007566.1:g.366_367del , LRG_39:g.366_367del
NG_009891.1:g.8035_8036del , LRG_37:g.8035_8036del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.958_959del
ENST00000695667.1:n.476_477del
ENST00000300692.9:c.406+65_406+66del MANE Select	ENSP00000300692.4:n.406+65_406+66del
ENST00000300692.8:c.406+65_406+66del	ENSP00000300692.4:n.406+65_406+66del
ENST00000392884.2:c.275-216_275-215del	ENSP00000376622.2:n.275-216_275-215del
ENST00000526561.1:n.80-216_80-215del
ENST00000529594.5:c.187+65_187+66del	ENSP00000437335.1:n.187+65_187+66del
ENST00000534687.5:c.288-216_288-215del
NM_000732.4:c.406+65_406+66del , LRG_37t1:c.406+65_406+66del	NP_000723.1:n.406+65_406+66del
NM_001040651.1:c.275-216_275-215del	NP_001035741.1:n.275-216_275-215del
NM_001040651.2:c.275-216_275-215del	NP_001035741.1:n.275-216_275-215del
NM_000732.6:c.406+65_406+66del MANE Select	NP_000723.1:n.406+65_406+66del