Canonical Allele Identifier: CA672356404

Gene: CD3D

Linked Data

• dbSNP Id: rs1364505791
• gnomAD v3: 11-118339743-AAC-A
• gnomAD v4: 11-118339743-AAC-A
• MyVariant Identifiers: chr11:g.118210459_118210460del (hg19) ; chr11:g.118339744_118339745del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339748_118339749del , CM000673.2:g.118339748_118339749del	GRCh38
NC_000011.9:g.118210463_118210464del , CM000673.1:g.118210463_118210464del	GRCh37
NC_000011.8:g.117715673_117715674del	NCBI36
NG_007566.1:g.405_406del , LRG_39:g.405_406del
NG_009891.1:g.8000_8001del , LRG_37:g.8000_8001del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.923_924del
ENST00000695667.1:n.441_442del
ENST00000695668.1:n.2421_2422del
ENST00000300692.9:c.406+30_406+31del MANE Select	ENSP00000300692.4:n.406+30_406+31del
ENST00000300692.8:c.406+30_406+31del	ENSP00000300692.4:n.406+30_406+31del
ENST00000392884.2:c.275-251_275-250del	ENSP00000376622.2:n.275-251_275-250del
ENST00000526561.1:n.80-251_80-250del
ENST00000529594.5:c.187+30_187+31del	ENSP00000437335.1:n.187+30_187+31del
ENST00000534687.5:c.288-251_288-250del
NM_000732.4:c.406+30_406+31del , LRG_37t1:c.406+30_406+31del	NP_000723.1:n.406+30_406+31del
NM_001040651.1:c.275-251_275-250del	NP_001035741.1:n.275-251_275-250del
NM_001040651.2:c.275-251_275-250del	NP_001035741.1:n.275-251_275-250del
NM_000732.6:c.406+30_406+31del MANE Select	NP_000723.1:n.406+30_406+31del