Canonical Allele Identifier: CA1821104908

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133520C= , CM000670.2:g.133133520C=	GRCh38
NC_000008.10:g.134145764C= , CM000670.1:g.134145764C=	GRCh37
NC_000008.9:g.134214946C=	NCBI36
NG_015832.1:g.271560C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8048C= MANE Select	ENSP00000220616.4:p.Thr2683=
ENST00000220616.8:c.8048C=	ENSP00000220616.4:p.Thr2683=
ENST00000519178.5:c.3414C=
ENST00000519543.5:c.2447C=	ENSP00000430430.1:p.Thr816=
ENST00000521107.1:c.260C=	ENSP00000430161.1:p.Thr87=
ENST00000522691.1:n.134C=
ENST00000523756.5:c.4703C=
NM_003235.4:c.8048C=	NP_003226.4:p.Thr2683=
XM_005251038.3:c.7856C=	XP_005251095.1:p.Thr2619=
XM_006716622.2:c.7985C=	XP_006716685.1:p.Thr2662=
XM_005251038.4:c.7856C=	XP_005251095.1:p.Thr2619=
XM_006716622.3:c.7985C=	XP_006716685.1:p.Thr2662=
XM_017013793.1:c.7982C=	XP_016869282.1:p.Thr2661=
XM_017013794.1:c.7913C=	XP_016869283.1:p.Thr2638=
XM_017013795.1:c.7877C=	XP_016869284.1:p.Thr2626=
XM_017013796.1:c.7829C=	XP_016869285.1:p.Thr2610=
XM_017013797.1:c.7787C=	XP_016869286.1:p.Thr2596=
NM_003235.5:c.8048C= MANE Select	NP_003226.4:p.Thr2683=