Canonical Allele Identifier: CA645557842

Gene: TG

Linked Data

• COSMIC: COSM1720675

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133541_133133542delinsTT , CM000670.2:g.133133541_133133542delinsTT	GRCh38
NC_000008.10:g.134145785_134145786delinsTT , CM000670.1:g.134145785_134145786delinsTT	GRCh37
NC_000008.9:g.134214967_134214968delinsTT	NCBI36
NG_015832.1:g.271581_271582delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8069_8070delinsTT MANE Select	ENSP00000220616.4:p.Pro2690Leu
ENST00000220616.8:c.8069_8070delinsTT	ENSP00000220616.4:p.Pro2690Leu
ENST00000519178.5:c.3435_3436delinsTT
ENST00000519543.5:c.2468_2469delinsTT	ENSP00000430430.1:p.Pro823Leu
ENST00000521107.1:c.281_282delinsTT	ENSP00000430161.1:p.Pro94Leu
ENST00000522691.1:n.155_156delinsTT
ENST00000523756.5:c.4724_4725delinsTT
NM_003235.4:c.8069_8070delinsTT	NP_003226.4:p.Pro2690Leu
XM_005251038.3:c.7877_7878delinsTT	XP_005251095.1:p.Pro2626Leu
XM_006716622.2:c.8006_8007delinsTT	XP_006716685.1:p.Pro2669Leu
XM_005251038.4:c.7877_7878delinsTT	XP_005251095.1:p.Pro2626Leu
XM_006716622.3:c.8006_8007delinsTT	XP_006716685.1:p.Pro2669Leu
XM_017013793.1:c.8003_8004delinsTT	XP_016869282.1:p.Pro2668Leu
XM_017013794.1:c.7934_7935delinsTT	XP_016869283.1:p.Pro2645Leu
XM_017013795.1:c.7898_7899delinsTT	XP_016869284.1:p.Pro2633Leu
XM_017013796.1:c.7850_7851delinsTT	XP_016869285.1:p.Pro2617Leu
XM_017013797.1:c.7808_7809delinsTT	XP_016869286.1:p.Pro2603Leu
NM_003235.5:c.8069_8070delinsTT MANE Select	NP_003226.4:p.Pro2690Leu