Canonical Allele Identifier: CA463017114

Gene: TG

Linked Data

• COSMIC: COSM5408868
• MyVariant Identifiers: chr8:g.134145786C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133542C>T , CM000670.2:g.133133542C>T	GRCh38
NC_000008.10:g.134145786C>T , CM000670.1:g.134145786C>T	GRCh37
NC_000008.9:g.134214968C>T	NCBI36
NG_015832.1:g.271582C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8070C>T MANE Select	ENSP00000220616.4:p.Pro2690=
ENST00000220616.8:c.8070C>T	ENSP00000220616.4:p.Pro2690=
ENST00000519178.5:c.3436C>T
ENST00000519543.5:c.2469C>T	ENSP00000430430.1:p.Pro823=
ENST00000521107.1:c.282C>T	ENSP00000430161.1:p.Pro94=
ENST00000522691.1:n.156C>T
ENST00000523756.5:c.4725C>T
NM_003235.4:c.8070C>T	NP_003226.4:p.Pro2690=
XM_005251038.3:c.7878C>T	XP_005251095.1:p.Pro2626=
XM_006716622.2:c.8007C>T	XP_006716685.1:p.Pro2669=
XM_005251038.4:c.7878C>T	XP_005251095.1:p.Pro2626=
XM_006716622.3:c.8007C>T	XP_006716685.1:p.Pro2669=
XM_017013793.1:c.8004C>T	XP_016869282.1:p.Pro2668=
XM_017013794.1:c.7935C>T	XP_016869283.1:p.Pro2645=
XM_017013795.1:c.7899C>T	XP_016869284.1:p.Pro2633=
XM_017013796.1:c.7851C>T	XP_016869285.1:p.Pro2617=
XM_017013797.1:c.7809C>T	XP_016869286.1:p.Pro2603=
NM_003235.5:c.8070C>T MANE Select	NP_003226.4:p.Pro2690=