Canonical Allele Identifier: CA463017066

Gene: TG

Linked Data

• COSMIC: COSM1455006
• MyVariant Identifiers: chr8:g.134145764del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133524del , CM000670.2:g.133133524del	GRCh38
NC_000008.10:g.134145768del , CM000670.1:g.134145768del	GRCh37
NC_000008.9:g.134214950del	NCBI36
NG_015832.1:g.271564del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8052del MANE Select	ENSP00000220616.4:p.Trp2685GlyfsTer26
ENST00000220616.8:c.8052del	ENSP00000220616.4:p.Trp2685GlyfsTer26
ENST00000519178.5:c.3418del
ENST00000519543.5:c.2451del	ENSP00000430430.1:p.Trp818GlyfsTer26
ENST00000521107.1:c.264del	ENSP00000430161.1:p.Trp89GlyfsTer26
ENST00000522691.1:n.138del
ENST00000523756.5:c.4707del
NM_003235.4:c.8052del	NP_003226.4:p.Trp2685GlyfsTer26
XM_005251038.3:c.7860del	XP_005251095.1:p.Trp2621GlyfsTer26
XM_006716622.2:c.7989del	XP_006716685.1:p.Trp2664GlyfsTer26
XM_005251038.4:c.7860del	XP_005251095.1:p.Trp2621GlyfsTer26
XM_006716622.3:c.7989del	XP_006716685.1:p.Trp2664GlyfsTer26
XM_017013793.1:c.7986del	XP_016869282.1:p.Trp2663GlyfsTer26
XM_017013794.1:c.7917del	XP_016869283.1:p.Trp2640GlyfsTer26
XM_017013795.1:c.7881del	XP_016869284.1:p.Trp2628GlyfsTer26
XM_017013796.1:c.7833del	XP_016869285.1:p.Trp2612GlyfsTer26
XM_017013797.1:c.7791del	XP_016869286.1:p.Trp2598GlyfsTer26
NM_003235.5:c.8052del MANE Select	NP_003226.4:p.Trp2685GlyfsTer26