Canonical Allele Identifier: CA1821104958

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133619C= , CM000670.2:g.133133619C=	GRCh38
NC_000008.10:g.134145863C= , CM000670.1:g.134145863C=	GRCh37
NC_000008.9:g.134215045C=	NCBI36
NG_015832.1:g.271659C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8147C= MANE Select	ENSP00000220616.4:p.Ser2716=
ENST00000220616.8:c.8147C=	ENSP00000220616.4:p.Ser2716=
ENST00000519178.5:c.3513C=
ENST00000519543.5:c.2546C=	ENSP00000430430.1:p.Ser849=
ENST00000521107.1:c.359C=	ENSP00000430161.1:p.Ser120=
ENST00000522691.1:n.233C=
ENST00000523756.5:c.4802C=
NM_003235.4:c.8147C=	NP_003226.4:p.Ser2716=
XM_005251038.3:c.7955C=	XP_005251095.1:p.Ser2652=
XM_006716622.2:c.8084C=	XP_006716685.1:p.Ser2695=
XM_005251038.4:c.7955C=	XP_005251095.1:p.Ser2652=
XM_006716622.3:c.8084C=	XP_006716685.1:p.Ser2695=
XM_017013793.1:c.8081C=	XP_016869282.1:p.Ser2694=
XM_017013794.1:c.8012C=	XP_016869283.1:p.Ser2671=
XM_017013795.1:c.7976C=	XP_016869284.1:p.Ser2659=
XM_017013796.1:c.7928C=	XP_016869285.1:p.Ser2643=
XM_017013797.1:c.7886C=	XP_016869286.1:p.Ser2629=
NM_003235.5:c.8147C= MANE Select	NP_003226.4:p.Ser2716=