Canonical Allele Identifier: CA229522384

Gene: CD3D

Linked Data

• dbSNP Id: rs867190354
• MyVariant Identifiers: chr11:g.118210519G>T (hg19) ; chr11:g.118339804G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339804G>T , CM000673.2:g.118339804G>T	GRCh38
NC_000011.9:g.118210519G>T , CM000673.1:g.118210519G>T	GRCh37
NC_000011.8:g.117715729G>T	NCBI36
NG_007566.1:g.461G>T , LRG_39:g.461G>T
NG_009891.1:g.7941C>A , LRG_37:g.7941C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695666.1:n.864C>A
ENST00000695667.1:n.382C>A
ENST00000695668.1:n.2362C>A
ENST00000300692.9:c.377C>A MANE Select	ENSP00000300692.4:p.Ala126Asp
ENST00000300692.8:c.377C>A	ENSP00000300692.4:p.Ala126Asp
ENST00000392884.2:c.275-310C>A	ENSP00000376622.2:n.275-310C>A
ENST00000526561.1:n.80-310C>A
ENST00000529594.5:c.158C>A	ENSP00000437335.1:p.Ala53Asp
ENST00000534687.5:c.288-310C>A
NM_000732.4:c.377C>A , LRG_37t1:c.377C>A	NP_000723.1:p.Ala126Asp
NM_001040651.1:c.275-310C>A	NP_001035741.1:n.275-310C>A
NM_001040651.2:c.275-310C>A	NP_001035741.1:n.275-310C>A
NM_000732.6:c.377C>A MANE Select	NP_000723.1:p.Ala126Asp