Canonical Allele Identifier: CA2616232451

Gene: CD3D

Linked Data

• dbSNP Id: rs2134059435
• gnomAD v4: 11-118339913-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339913G>A , CM000673.2:g.118339913G>A	GRCh38
NC_000011.9:g.118210628G>A , CM000673.1:g.118210628G>A	GRCh37
NC_000011.8:g.117715838G>A	NCBI36
NG_007566.1:g.570G>A , LRG_39:g.570G>A
NG_009891.1:g.7832C>T , LRG_37:g.7832C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.755C>T
ENST00000695667.1:n.280-7C>T
ENST00000695668.1:n.2260-7C>T
ENST00000300692.9:c.275-7C>T MANE Select	ENSP00000300692.4:n.275-7C>T
ENST00000300692.8:c.275-7C>T	ENSP00000300692.4:n.275-7C>T
ENST00000392884.2:c.275-419C>T	ENSP00000376622.2:n.275-419C>T
ENST00000526561.1:n.80-419C>T
ENST00000529594.5:c.56-7C>T	ENSP00000437335.1:n.56-7C>T
ENST00000534687.5:c.288-419C>T
NM_000732.4:c.275-7C>T , LRG_37t1:c.275-7C>T	NP_000723.1:n.275-7C>T
NM_001040651.1:c.275-419C>T	NP_001035741.1:n.275-419C>T
NM_001040651.2:c.275-419C>T	NP_001035741.1:n.275-419C>T
NM_000732.6:c.275-7C>T MANE Select	NP_000723.1:n.275-7C>T