Canonical Allele Identifier: CA2616232448

Gene: CD3D

Linked Data

• gnomAD v4: 11-118339856-CAAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339857_118339859del , CM000673.2:g.118339857_118339859del	GRCh38
NC_000011.9:g.118210572_118210574del , CM000673.1:g.118210572_118210574del	GRCh37
NC_000011.8:g.117715782_117715784del	NCBI36
NG_007566.1:g.514_516del , LRG_39:g.514_516del
NG_009891.1:g.7886_7888del , LRG_37:g.7886_7888del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.809_811del
ENST00000695667.1:n.327_329del
ENST00000695668.1:n.2307_2309del
ENST00000300692.9:c.322_324del MANE Select	ENSP00000300692.4:p.Ile108del
ENST00000300692.8:c.322_324del	ENSP00000300692.4:p.Ile108del
ENST00000392884.2:c.275-365_275-363del	ENSP00000376622.2:n.275-365_275-363del
ENST00000526561.1:n.80-365_80-363del
ENST00000529594.5:c.103_105del	ENSP00000437335.1:p.Ile35del
ENST00000534687.5:c.288-365_288-363del
NM_000732.4:c.322_324del , LRG_37t1:c.322_324del	NP_000723.1:p.Ile108del
NM_001040651.1:c.275-365_275-363del	NP_001035741.1:n.275-365_275-363del
NM_001040651.2:c.275-365_275-363del	NP_001035741.1:n.275-365_275-363del
NM_000732.6:c.322_324del MANE Select	NP_000723.1:p.Ile108del