Canonical Allele Identifier: CA382788271

Gene: CD3D

Linked Data

• gnomAD v4: 11-118339846-A-G
• MyVariant Identifiers: chr11:g.118210561A>G (hg19) ; chr11:g.118339846A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339846A>G , CM000673.2:g.118339846A>G	GRCh38
NC_000011.9:g.118210561A>G , CM000673.1:g.118210561A>G	GRCh37
NC_000011.8:g.117715771A>G	NCBI36
NG_007566.1:g.503A>G , LRG_39:g.503A>G
NG_009891.1:g.7899T>C , LRG_37:g.7899T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.822T>C
ENST00000695667.1:n.340T>C
ENST00000695668.1:n.2320T>C
ENST00000300692.9:c.335T>C MANE Select	ENSP00000300692.4:p.Val112Ala
ENST00000300692.8:c.335T>C	ENSP00000300692.4:p.Val112Ala
ENST00000392884.2:c.275-352T>C	ENSP00000376622.2:n.275-352T>C
ENST00000526561.1:n.80-352T>C
ENST00000529594.5:c.116T>C	ENSP00000437335.1:p.Val39Ala
ENST00000534687.5:c.288-352T>C
NM_000732.4:c.335T>C , LRG_37t1:c.335T>C	NP_000723.1:p.Val112Ala
NM_001040651.1:c.275-352T>C	NP_001035741.1:n.275-352T>C
NM_001040651.2:c.275-352T>C	NP_001035741.1:n.275-352T>C
NM_000732.6:c.335T>C MANE Select	NP_000723.1:p.Val112Ala