Canonical Allele Identifier: CA1821104917

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133539_133133540delinsAC , CM000670.2:g.133133539_133133540delinsAC	GRCh38
NC_000008.10:g.134145783_134145784delinsAC , CM000670.1:g.134145783_134145784delinsAC	GRCh37
NC_000008.9:g.134214965_134214966delinsAC	NCBI36
NG_015832.1:g.271579_271580delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8067_8068delinsAC MANE Select	ENSP00000220616.4:p.Val2689=
ENST00000220616.8:c.8067_8068delinsAC	ENSP00000220616.4:p.Val2689=
ENST00000519178.5:c.3433_3434delinsAC
ENST00000519543.5:c.2466_2467delinsAC	ENSP00000430430.1:p.Val822=
ENST00000521107.1:c.279_280delinsAC	ENSP00000430161.1:p.Val93=
ENST00000522691.1:n.153_154delinsAC
ENST00000523756.5:c.4722_4723delinsAC
NM_003235.4:c.8067_8068delinsAC	NP_003226.4:p.Val2689=
XM_005251038.3:c.7875_7876delinsAC	XP_005251095.1:p.Val2625=
XM_006716622.2:c.8004_8005delinsAC	XP_006716685.1:p.Val2668=
XM_005251038.4:c.7875_7876delinsAC	XP_005251095.1:p.Val2625=
XM_006716622.3:c.8004_8005delinsAC	XP_006716685.1:p.Val2668=
XM_017013793.1:c.8001_8002delinsAC	XP_016869282.1:p.Val2667=
XM_017013794.1:c.7932_7933delinsAC	XP_016869283.1:p.Val2644=
XM_017013795.1:c.7896_7897delinsAC	XP_016869284.1:p.Val2632=
XM_017013796.1:c.7848_7849delinsAC	XP_016869285.1:p.Val2616=
XM_017013797.1:c.7806_7807delinsAC	XP_016869286.1:p.Val2602=
NM_003235.5:c.8067_8068delinsAC MANE Select	NP_003226.4:p.Val2689=