Canonical Allele Identifier: CA2003459099
Community Standard Title: NM_000073.3(CD3G):c.1A= (p.Met1=)
Gene: CD3G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118344424A= , CM000673.2:g.118344424A= GRCh38
NC_000011.9:g.118215139A= , CM000673.1:g.118215139A= GRCh37
NC_000011.8:g.117720349A= NCBI36
NG_007566.1:g.5081A= , LRG_39:g.5081A=
NG_009891.1:g.3321T= , LRG_37:g.3321T=

Transcript Alleles

HGVS Amino-acid Change
NM_000073.3:c.1A= MANE Select NP_000064.1:p.Met1=
ENST00000532917.3:c.1A= MANE Select ENSP00000431445.2:p.Met1=
NM_000073.2:c.1A= , LRG_39t1:c.1A= NP_000064.1:p.Met1=
ENST00000292144.8:c.1A= ENSP00000292144.4:p.Met1=
ENST00000392883.6:c.-180A= ENSP00000376621.2:n.-180A=
ENST00000527777.5:n.81A=
ENST00000528540.5:n.39A=
ENST00000532903.1:n.18A=
ENST00000532917.1:c.1A= ENSP00000431445.1:p.Met1=
ENST00000533462.5:n.81A=
XM_005271724.2:c.1A= XP_005271781.1:p.Met1=
XM_005271724.4:c.1A= XP_005271781.1:p.Met1=
XM_006718941.2:c.1A= XP_006719004.1:p.Met1=
XM_006718941.3:c.1A= XP_006719004.1:p.Met1=