Canonical Allele Identifier: CA1821104984

Gene: TG

Linked Data

• dbSNP Id: rs1852119141

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133668_133133669insT , CM000670.2:g.133133668_133133669insT	GRCh38
NC_000008.10:g.134145912_134145913insT , CM000670.1:g.134145912_134145913insT	GRCh37
NC_000008.9:g.134215094_134215095insT	NCBI36
NG_015832.1:g.271708_271709insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8188+8_8188+9insT MANE Select	ENSP00000220616.4:n.8188+8_8188+9insT
ENST00000220616.8:c.8188+8_8188+9insT	ENSP00000220616.4:n.8188+8_8188+9insT
ENST00000519178.5:c.3554+8_3554+9insT
ENST00000519543.5:c.2587+8_2587+9insT	ENSP00000430430.1:n.2587+8_2587+9insT
ENST00000521107.1:c.400+8_400+9insT	ENSP00000430161.1:n.400+8_400+9insT
ENST00000522691.1:n.274+8_274+9insT
ENST00000523756.5:c.4843+8_4843+9insT
NM_003235.4:c.8188+8_8188+9insT	NP_003226.4:n.8188+8_8188+9insT
XM_005251038.3:c.7996+8_7996+9insT	XP_005251095.1:n.7996+8_7996+9insT
XM_006716622.2:c.8125+8_8125+9insT	XP_006716685.1:n.8125+8_8125+9insT
XM_005251038.4:c.7996+8_7996+9insT	XP_005251095.1:n.7996+8_7996+9insT
XM_006716622.3:c.8125+8_8125+9insT	XP_006716685.1:n.8125+8_8125+9insT
XM_017013793.1:c.8122+8_8122+9insT	XP_016869282.1:n.8122+8_8122+9insT
XM_017013794.1:c.8053+8_8053+9insT	XP_016869283.1:n.8053+8_8053+9insT
XM_017013795.1:c.8017+8_8017+9insT	XP_016869284.1:n.8017+8_8017+9insT
XM_017013796.1:c.7969+8_7969+9insT	XP_016869285.1:n.7969+8_7969+9insT
XM_017013797.1:c.7927+8_7927+9insT	XP_016869286.1:n.7927+8_7927+9insT
NM_003235.5:c.8188+8_8188+9insT MANE Select	NP_003226.4:n.8188+8_8188+9insT