Canonical Allele Identifier: CA382792298

Gene: CD3G

Linked Data

• gnomAD v4: 11-118349778-G-T
• MyVariant Identifiers: chr11:g.118220493G>T (hg19) ; chr11:g.118349778G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118349778G>T , CM000673.2:g.118349778G>T	GRCh38
NC_000011.9:g.118220493G>T , CM000673.1:g.118220493G>T	GRCh37
NC_000011.8:g.117725703G>T	NCBI36
NG_007566.1:g.10435G>T , LRG_39:g.10435G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000532917.3:c.115G>T MANE Select	ENSP00000431445.2:p.Asp39Tyr
ENST00000292144.8:c.*172G>T	ENSP00000292144.4:n.*172G>T
ENST00000392883.6:c.-66G>T	ENSP00000376621.2:n.-66G>T
ENST00000527777.5:n.195G>T
ENST00000528540.5:n.136G>T
ENST00000532903.1:n.191G>T
ENST00000532917.1:c.115G>T	ENSP00000431445.1:p.Asp39Tyr
ENST00000533462.5:n.887G>T
NM_000073.2:c.115G>T , LRG_39t1:c.115G>T	NP_000064.1:p.Asp39Tyr
XM_005271724.2:c.115G>T	XP_005271781.1:p.Asp39Tyr
XM_006718941.2:c.115G>T	XP_006719004.1:p.Asp39Tyr
XM_005271724.4:c.115G>T	XP_005271781.1:p.Asp39Tyr
XM_006718941.3:c.115G>T	XP_006719004.1:p.Asp39Tyr
NM_000073.3:c.115G>T MANE Select	NP_000064.1:p.Asp39Tyr