Canonical Allele Identifier: CA2725025486

Gene: CD3D

Linked Data

• dbSNP Id: rs2134059112

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339719_118339720insGCAC , CM000673.2:g.118339719_118339720insGCAC	GRCh38
NC_000011.9:g.118210434_118210435insGCAC , CM000673.1:g.118210434_118210435insGCAC	GRCh37
NC_000011.8:g.117715644_117715645insGCAC	NCBI36
NG_007566.1:g.376_377insGCAC , LRG_39:g.376_377insGCAC
NG_009891.1:g.8028_8029insCGTG , LRG_37:g.8028_8029insCGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.951_952insCGTG
ENST00000695667.1:n.469_470insCGTG
ENST00000300692.9:c.406+58_406+59insCGTG MANE Select	ENSP00000300692.4:n.406+58_406+59insCGTG
ENST00000300692.8:c.406+58_406+59insCGTG	ENSP00000300692.4:n.406+58_406+59insCGTG
ENST00000392884.2:c.275-223_275-222insCGTG	ENSP00000376622.2:n.275-223_275-222insCGTG
ENST00000526561.1:n.80-223_80-222insCGTG
ENST00000529594.5:c.187+58_187+59insCGTG	ENSP00000437335.1:n.187+58_187+59insCGTG
ENST00000534687.5:c.288-223_288-222insCGTG
NM_000732.4:c.406+58_406+59insCGTG , LRG_37t1:c.406+58_406+59insCGTG	NP_000723.1:n.406+58_406+59insCGTG
NM_001040651.1:c.275-223_275-222insCGTG	NP_001035741.1:n.275-223_275-222insCGTG
NM_001040651.2:c.275-223_275-222insCGTG	NP_001035741.1:n.275-223_275-222insCGTG
NM_000732.6:c.406+58_406+59insCGTG MANE Select	NP_000723.1:n.406+58_406+59insCGTG