Canonical Allele Identifier: CA382792837
Community Standard Title: NM_000073.3(CD3G):c.271C>T (p.Gln91Ter)
Gene: CD3G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118349934C>T , CM000673.2:g.118349934C>T GRCh38
NC_000011.9:g.118220649C>T , CM000673.1:g.118220649C>T GRCh37
NC_000011.8:g.117725859C>T NCBI36
NG_007566.1:g.10591C>T , LRG_39:g.10591C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000073.3:c.271C>T MANE Select NP_000064.1:p.Gln91Ter
ENST00000532917.3:c.271C>T MANE Select ENSP00000431445.2:p.Gln91Ter
NM_000073.2:c.271C>T , LRG_39t1:c.271C>T NP_000064.1:p.Gln91Ter
ENST00000292144.8:c.*328C>T ENSP00000292144.4:n.*328C>T
ENST00000392883.6:c.91C>T ENSP00000376621.2:p.Gln31Ter
ENST00000527777.5:n.351C>T
ENST00000532903.1:n.347C>T
ENST00000532917.1:c.271C>T ENSP00000431445.1:p.Gln91Ter
ENST00000533462.5:n.1043C>T
XM_005271724.2:c.271C>T XP_005271781.1:p.Gln91Ter
XM_005271724.4:c.271C>T XP_005271781.1:p.Gln91Ter
XM_006718941.2:c.271C>T XP_006719004.1:p.Gln91Ter
XM_006718941.3:c.271C>T XP_006719004.1:p.Gln91Ter