Canonical Allele Identifier: CA382788404

Gene: CD3D

Linked Data

• gnomAD v4: 11-118339883-C-T
• MyVariant Identifiers: chr11:g.118210598C>T (hg19) ; chr11:g.118339883C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339883C>T , CM000673.2:g.118339883C>T	GRCh38
NC_000011.9:g.118210598C>T , CM000673.1:g.118210598C>T	GRCh37
NC_000011.8:g.117715808C>T	NCBI36
NG_007566.1:g.540C>T , LRG_39:g.540C>T
NG_009891.1:g.7862G>A , LRG_37:g.7862G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.785G>A
ENST00000695667.1:n.303G>A
ENST00000695668.1:n.2283G>A
ENST00000300692.9:c.298G>A MANE Select	ENSP00000300692.4:p.Asp100Asn
ENST00000300692.8:c.298G>A	ENSP00000300692.4:p.Asp100Asn
ENST00000392884.2:c.275-389G>A	ENSP00000376622.2:n.275-389G>A
ENST00000526561.1:n.80-389G>A
ENST00000529594.5:c.79G>A	ENSP00000437335.1:p.Asp27Asn
ENST00000534687.5:c.288-389G>A
NM_000732.4:c.298G>A , LRG_37t1:c.298G>A	NP_000723.1:p.Asp100Asn
NM_001040651.1:c.275-389G>A	NP_001035741.1:n.275-389G>A
NM_001040651.2:c.275-389G>A	NP_001035741.1:n.275-389G>A
NM_000732.6:c.298G>A MANE Select	NP_000723.1:p.Asp100Asn