Canonical Allele Identifier: CA2003456924

Gene: CD3D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339646_118339647delinsAC , CM000673.2:g.118339646_118339647delinsAC	GRCh38
NC_000011.9:g.118210361_118210362delinsAC , CM000673.1:g.118210361_118210362delinsAC	GRCh37
NC_000011.8:g.117715571_117715572delinsAC	NCBI36
NG_007566.1:g.303_304delinsAC , LRG_39:g.303_304delinsAC
NG_009891.1:g.8098_8099delinsGT , LRG_37:g.8098_8099delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.1021_1022delinsGT
ENST00000695667.1:n.539_540delinsGT
ENST00000300692.9:c.406+128_406+129delinsGT MANE Select	ENSP00000300692.4:n.406+128_406+129delinsGT
ENST00000300692.8:c.406+128_406+129delinsGT	ENSP00000300692.4:n.406+128_406+129delinsGT
ENST00000392884.2:c.275-153_275-152delinsGT	ENSP00000376622.2:n.275-153_275-152delinsGT
ENST00000526561.1:n.80-153_80-152delinsGT
ENST00000529594.5:c.187+128_187+129delinsGT	ENSP00000437335.1:n.187+128_187+129delinsGT
ENST00000534687.5:c.288-153_288-152delinsGT
NM_000732.4:c.406+128_406+129delinsGT , LRG_37t1:c.406+128_406+129delinsGT	NP_000723.1:n.406+128_406+129delinsGT
NM_001040651.1:c.275-153_275-152delinsGT	NP_001035741.1:n.275-153_275-152delinsGT
NM_001040651.2:c.275-153_275-152delinsGT	NP_001035741.1:n.275-153_275-152delinsGT
NM_000732.6:c.406+128_406+129delinsGT MANE Select	NP_000723.1:n.406+128_406+129delinsGT