Canonical Allele Identifier: CA382792295

Gene: CD3G

Linked Data

• MyVariant Identifiers: chr11:g.118220492A>C (hg19) ; chr11:g.118349777A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118349777A>C , CM000673.2:g.118349777A>C	GRCh38
NC_000011.9:g.118220492A>C , CM000673.1:g.118220492A>C	GRCh37
NC_000011.8:g.117725702A>C	NCBI36
NG_007566.1:g.10434A>C , LRG_39:g.10434A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000532917.3:c.114A>C MANE Select	ENSP00000431445.2:p.Glu38Asp
ENST00000292144.8:c.*171A>C	ENSP00000292144.4:n.*171A>C
ENST00000392883.6:c.-67A>C	ENSP00000376621.2:n.-67A>C
ENST00000527777.5:n.194A>C
ENST00000528540.5:n.135A>C
ENST00000532903.1:n.190A>C
ENST00000532917.1:c.114A>C	ENSP00000431445.1:p.Glu38Asp
ENST00000533462.5:n.886A>C
NM_000073.2:c.114A>C , LRG_39t1:c.114A>C	NP_000064.1:p.Glu38Asp
XM_005271724.2:c.114A>C	XP_005271781.1:p.Glu38Asp
XM_006718941.2:c.114A>C	XP_006719004.1:p.Glu38Asp
XM_005271724.4:c.114A>C	XP_005271781.1:p.Glu38Asp
XM_006718941.3:c.114A>C	XP_006719004.1:p.Glu38Asp
NM_000073.3:c.114A>C MANE Select	NP_000064.1:p.Glu38Asp