Canonical Allele Identifier: CA2003456944

Gene: CD3D

Linked Data

• dbSNP Id: rs1948281599

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339704dup , CM000673.2:g.118339704dup	GRCh38
NC_000011.9:g.118210419dup , CM000673.1:g.118210419dup	GRCh37
NC_000011.8:g.117715629dup	NCBI36
NG_007566.1:g.361dup , LRG_39:g.361dup
NG_009891.1:g.8041dup , LRG_37:g.8041dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.964dup
ENST00000695667.1:n.482dup
ENST00000300692.9:c.406+71dup MANE Select	ENSP00000300692.4:n.406+71dup
ENST00000300692.8:c.406+71dup	ENSP00000300692.4:n.406+71dup
ENST00000392884.2:c.275-210dup	ENSP00000376622.2:n.275-210dup
ENST00000526561.1:n.80-210dup
ENST00000529594.5:c.187+71dup	ENSP00000437335.1:n.187+71dup
ENST00000534687.5:c.288-210dup
NM_000732.4:c.406+71dup , LRG_37t1:c.406+71dup	NP_000723.1:n.406+71dup
NM_001040651.1:c.275-210dup	NP_001035741.1:n.275-210dup
NM_001040651.2:c.275-210dup	NP_001035741.1:n.275-210dup
NM_000732.6:c.406+71dup MANE Select	NP_000723.1:n.406+71dup