Canonical Allele Identifier: CA382789090
Community Standard Title: NM_000732.6(CD3D):c.237C>G (p.Tyr79Ter)
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118340412G>C , CM000673.2:g.118340412G>C GRCh38
NC_000011.9:g.118211127G>C , CM000673.1:g.118211127G>C GRCh37
NC_000011.8:g.117716337G>C NCBI36
NG_007566.1:g.1069G>C , LRG_39:g.1069G>C
NG_009891.1:g.7333C>G , LRG_37:g.7333C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000732.6:c.237C>G MANE Select NP_000723.1:p.Tyr79Ter
ENST00000300692.9:c.237C>G MANE Select ENSP00000300692.4:p.Tyr79Ter
NM_000732.4:c.237C>G , LRG_37t1:c.237C>G NP_000723.1:p.Tyr79Ter
NM_001040651.1:c.237C>G NP_001035741.1:p.Tyr79Ter
NM_001040651.2:c.237C>G NP_001035741.1:p.Tyr79Ter
ENST00000300692.8:c.237C>G ENSP00000300692.4:p.Tyr79Ter
ENST00000392884.2:c.237C>G ENSP00000376622.2:p.Tyr79Ter
ENST00000526561.1:n.80-918C>G
ENST00000529594.5:c.56-506C>G ENSP00000437335.1:n.56-506C>G
ENST00000534687.5:c.250C>G
ENST00000695666.1:n.256C>G
ENST00000695667.1:n.242C>G
ENST00000695668.1:n.2222C>G