Canonical Allele Identifier: CA2793810955

Gene: CD3D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339718_118339719insTA , CM000673.2:g.118339718_118339719insTA	GRCh38
NC_000011.9:g.118210433_118210434insTA , CM000673.1:g.118210433_118210434insTA	GRCh37
NC_000011.8:g.117715643_117715644insTA	NCBI36
NG_007566.1:g.375_376insTA , LRG_39:g.375_376insTA
NG_009891.1:g.8027_8028insAT , LRG_37:g.8027_8028insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.950_951insAT
ENST00000695667.1:n.468_469insAT
ENST00000300692.9:c.406+57_406+58insAT MANE Select	ENSP00000300692.4:n.406+57_406+58insAT
ENST00000300692.8:c.406+57_406+58insAT	ENSP00000300692.4:n.406+57_406+58insAT
ENST00000392884.2:c.275-224_275-223insAT	ENSP00000376622.2:n.275-224_275-223insAT
ENST00000526561.1:n.80-224_80-223insAT
ENST00000529594.5:c.187+57_187+58insAT	ENSP00000437335.1:n.187+57_187+58insAT
ENST00000534687.5:c.288-224_288-223insAT
NM_000732.4:c.406+57_406+58insAT , LRG_37t1:c.406+57_406+58insAT	NP_000723.1:n.406+57_406+58insAT
NM_001040651.1:c.275-224_275-223insAT	NP_001035741.1:n.275-224_275-223insAT
NM_001040651.2:c.275-224_275-223insAT	NP_001035741.1:n.275-224_275-223insAT
NM_000732.6:c.406+57_406+58insAT MANE Select	NP_000723.1:n.406+57_406+58insAT