Canonical Allele Identifier: CA382792282

Gene: CD3G

Linked Data

• MyVariant Identifiers: chr11:g.118220487C>G (hg19) ; chr11:g.118349772C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118349772C>G , CM000673.2:g.118349772C>G	GRCh38
NC_000011.9:g.118220487C>G , CM000673.1:g.118220487C>G	GRCh37
NC_000011.8:g.117725697C>G	NCBI36
NG_007566.1:g.10429C>G , LRG_39:g.10429C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000532917.3:c.109C>G MANE Select	ENSP00000431445.2:p.Gln37Glu
ENST00000292144.8:c.*166C>G	ENSP00000292144.4:n.*166C>G
ENST00000392883.6:c.-72C>G	ENSP00000376621.2:n.-72C>G
ENST00000527777.5:n.189C>G
ENST00000528540.5:n.130C>G
ENST00000532903.1:n.185C>G
ENST00000532917.1:c.109C>G	ENSP00000431445.1:p.Gln37Glu
ENST00000533462.5:n.881C>G
NM_000073.2:c.109C>G , LRG_39t1:c.109C>G	NP_000064.1:p.Gln37Glu
XM_005271724.2:c.109C>G	XP_005271781.1:p.Gln37Glu
XM_006718941.2:c.109C>G	XP_006719004.1:p.Gln37Glu
XM_005271724.4:c.109C>G	XP_005271781.1:p.Gln37Glu
XM_006718941.3:c.109C>G	XP_006719004.1:p.Gln37Glu
NM_000073.3:c.109C>G MANE Select	NP_000064.1:p.Gln37Glu