Canonical Allele Identifier: CA918978574

Gene: CD3D

Linked Data

• dbSNP Id: rs1591277802

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339781_118339784del , CM000673.2:g.118339781_118339784del	GRCh38
NC_000011.9:g.118210496_118210499del , CM000673.1:g.118210496_118210499del	GRCh37
NC_000011.8:g.117715706_117715709del	NCBI36
NG_007566.1:g.438_441del , LRG_39:g.438_441del
NG_009891.1:g.7964_7967del , LRG_37:g.7964_7967del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.887_890del
ENST00000695667.1:n.405_408del
ENST00000695668.1:n.2385_2388del
ENST00000300692.9:c.400_403del MANE Select	ENSP00000300692.4:p.Ser134GlyfsTer9
ENST00000300692.8:c.400_403del	ENSP00000300692.4:p.Ser134GlyfsTer9
ENST00000392884.2:c.275-287_275-284del	ENSP00000376622.2:n.275-287_275-284del
ENST00000526561.1:n.80-287_80-284del
ENST00000529594.5:c.181_184del	ENSP00000437335.1:p.Ser61GlyfsTer9
ENST00000534687.5:c.288-287_288-284del
NM_000732.4:c.400_403del , LRG_37t1:c.400_403del	NP_000723.1:p.Ser134GlyfsTer9
NM_001040651.1:c.275-287_275-284del	NP_001035741.1:n.275-287_275-284del
NM_001040651.2:c.275-287_275-284del	NP_001035741.1:n.275-287_275-284del
NM_000732.6:c.400_403del MANE Select	NP_000723.1:p.Ser134GlyfsTer9