Canonical Allele Identifier: CA382788082

Gene: CD3D

Linked Data

• dbSNP Id: rs1270882114
• MyVariant Identifiers: chr11:g.118210507G>A (hg19) ; chr11:g.118339792G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339792G>A , CM000673.2:g.118339792G>A	GRCh38
NC_000011.9:g.118210507G>A , CM000673.1:g.118210507G>A	GRCh37
NC_000011.8:g.117715717G>A	NCBI36
NG_007566.1:g.449G>A , LRG_39:g.449G>A
NG_009891.1:g.7953C>T , LRG_37:g.7953C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.876C>T
ENST00000695667.1:n.394C>T
ENST00000695668.1:n.2374C>T
ENST00000300692.9:c.389C>T MANE Select	ENSP00000300692.4:p.Thr130Ile
ENST00000300692.8:c.389C>T	ENSP00000300692.4:p.Thr130Ile
ENST00000392884.2:c.275-298C>T	ENSP00000376622.2:n.275-298C>T
ENST00000526561.1:n.80-298C>T
ENST00000529594.5:c.170C>T	ENSP00000437335.1:p.Thr57Ile
ENST00000534687.5:c.288-298C>T
NM_000732.4:c.389C>T , LRG_37t1:c.389C>T	NP_000723.1:p.Thr130Ile
NM_001040651.1:c.275-298C>T	NP_001035741.1:n.275-298C>T
NM_001040651.2:c.275-298C>T	NP_001035741.1:n.275-298C>T
NM_000732.6:c.389C>T MANE Select	NP_000723.1:p.Thr130Ile