Canonical Allele Identifier: CA372233914

Gene: TG

Linked Data

• COSMIC: COSM1096321
• MyVariant Identifiers: chr8:g.134030233G>T (hg19) ; chr8:g.133017988G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017988G>T , CM000670.2:g.133017988G>T	GRCh38
NC_000008.10:g.134030233G>T , CM000670.1:g.134030233G>T	GRCh37
NC_000008.9:g.134099415G>T	NCBI36
NG_015832.1:g.156029G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6773G>T MANE Select	ENSP00000220616.4:p.Ser2258Ile
ENST00000220616.8:c.6773G>T	ENSP00000220616.4:p.Ser2258Ile
ENST00000518108.1:c.168+122G>T
ENST00000519178.5:c.2139G>T
ENST00000519543.5:c.1172G>T	ENSP00000430430.1:p.Ser391Ile
ENST00000523756.5:c.3428G>T
NM_003235.4:c.6773G>T	NP_003226.4:p.Ser2258Ile
XM_005251038.3:c.6581G>T	XP_005251095.1:p.Ser2194Ile
XM_006716622.2:c.6710G>T	XP_006716685.1:p.Ser2237Ile
XM_005251038.4:c.6581G>T	XP_005251095.1:p.Ser2194Ile
XM_006716622.3:c.6710G>T	XP_006716685.1:p.Ser2237Ile
XM_017013793.1:c.6707G>T	XP_016869282.1:p.Ser2236Ile
XM_017013794.1:c.6773G>T	XP_016869283.1:p.Ser2258Ile
XM_017013795.1:c.6602G>T	XP_016869284.1:p.Ser2201Ile
XM_017013796.1:c.6554G>T	XP_016869285.1:p.Ser2185Ile
XM_017013797.1:c.6512G>T	XP_016869286.1:p.Ser2171Ile
XM_017013798.1:c.6773G>T	XP_016869287.1:p.Ser2258Ile
NM_003235.5:c.6773G>T MANE Select	NP_003226.4:p.Ser2258Ile