Canonical Allele Identifier: CA1821104907

Gene: TG

Linked Data

• dbSNP Id: rs1852105322

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133518_133133519insCTCGGT , CM000670.2:g.133133518_133133519insCTCGGT	GRCh38
NC_000008.10:g.134145762_134145763insCTCGGT , CM000670.1:g.134145762_134145763insCTCGGT	GRCh37
NC_000008.9:g.134214944_134214945insCTCGGT	NCBI36
NG_015832.1:g.271558_271559insCTCGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8046_8047insCTCGGT MANE Select	ENSP00000220616.4:p.Ala2682_Thr2683insLeuGly
ENST00000220616.8:c.8046_8047insCTCGGT	ENSP00000220616.4:p.Ala2682_Thr2683insLeuGly
ENST00000519178.5:c.3412_3413insCTCGGT
ENST00000519543.5:c.2445_2446insCTCGGT	ENSP00000430430.1:p.Ala815_Thr816insLeuGly
ENST00000521107.1:c.258_259insCTCGGT	ENSP00000430161.1:p.Ala86_Thr87insLeuGly
ENST00000522691.1:n.132_133insCTCGGT
ENST00000523756.5:c.4701_4702insCTCGGT
NM_003235.4:c.8046_8047insCTCGGT	NP_003226.4:p.Ala2682_Thr2683insLeuGly
XM_005251038.3:c.7854_7855insCTCGGT	XP_005251095.1:p.Ala2618_Thr2619insLeuGly
XM_006716622.2:c.7983_7984insCTCGGT	XP_006716685.1:p.Ala2661_Thr2662insLeuGly
XM_005251038.4:c.7854_7855insCTCGGT	XP_005251095.1:p.Ala2618_Thr2619insLeuGly
XM_006716622.3:c.7983_7984insCTCGGT	XP_006716685.1:p.Ala2661_Thr2662insLeuGly
XM_017013793.1:c.7980_7981insCTCGGT	XP_016869282.1:p.Ala2660_Thr2661insLeuGly
XM_017013794.1:c.7911_7912insCTCGGT	XP_016869283.1:p.Ala2637_Thr2638insLeuGly
XM_017013795.1:c.7875_7876insCTCGGT	XP_016869284.1:p.Ala2625_Thr2626insLeuGly
XM_017013796.1:c.7827_7828insCTCGGT	XP_016869285.1:p.Ala2609_Thr2610insLeuGly
XM_017013797.1:c.7785_7786insCTCGGT	XP_016869286.1:p.Ala2595_Thr2596insLeuGly
NM_003235.5:c.8046_8047insCTCGGT MANE Select	NP_003226.4:p.Ala2682_Thr2683insLeuGly