Canonical Allele Identifier: CA2003457080

Gene: CD3D

Linked Data

• ClinVar Variation Id: 2802159
• ClinVar RCV Id: RCV003745915
• dbSNP Id: rs202156183

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339915G>A , CM000673.2:g.118339915G>A	GRCh38
NC_000011.9:g.118210630G>A , CM000673.1:g.118210630G>A	GRCh37
NC_000011.8:g.117715840G>A	NCBI36
NG_007566.1:g.572G>A , LRG_39:g.572G>A
NG_009891.1:g.7830C>T , LRG_37:g.7830C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695666.1:n.753C>T
ENST00000695667.1:n.280-9C>T
ENST00000695668.1:n.2260-9C>T
ENST00000300692.9:c.275-9C>T MANE Select	ENSP00000300692.4:n.275-9C>T
ENST00000300692.8:c.275-9C>T	ENSP00000300692.4:n.275-9C>T
ENST00000392884.2:c.275-421C>T	ENSP00000376622.2:n.275-421C>T
ENST00000526561.1:n.80-421C>T
ENST00000529594.5:c.56-9C>T	ENSP00000437335.1:n.56-9C>T
ENST00000534687.5:c.288-421C>T
NM_000732.4:c.275-9C>T , LRG_37t1:c.275-9C>T	NP_000723.1:n.275-9C>T
NM_001040651.1:c.275-421C>T	NP_001035741.1:n.275-421C>T
NM_001040651.2:c.275-421C>T	NP_001035741.1:n.275-421C>T
NM_000732.6:c.275-9C>T MANE Select	NP_000723.1:n.275-9C>T