Canonical Allele Identifier: CA1821104963

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133628C= , CM000670.2:g.133133628C=	GRCh38
NC_000008.10:g.134145872C= , CM000670.1:g.134145872C=	GRCh37
NC_000008.9:g.134215054C=	NCBI36
NG_015832.1:g.271668C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8156C= MANE Select	ENSP00000220616.4:p.Ser2719=
ENST00000220616.8:c.8156C=	ENSP00000220616.4:p.Ser2719=
ENST00000519178.5:c.3522C=
ENST00000519543.5:c.2555C=	ENSP00000430430.1:p.Ser852=
ENST00000521107.1:c.368C=	ENSP00000430161.1:p.Ser123=
ENST00000522691.1:n.242C=
ENST00000523756.5:c.4811C=
NM_003235.4:c.8156C=	NP_003226.4:p.Ser2719=
XM_005251038.3:c.7964C=	XP_005251095.1:p.Ser2655=
XM_006716622.2:c.8093C=	XP_006716685.1:p.Ser2698=
XM_005251038.4:c.7964C=	XP_005251095.1:p.Ser2655=
XM_006716622.3:c.8093C=	XP_006716685.1:p.Ser2698=
XM_017013793.1:c.8090C=	XP_016869282.1:p.Ser2697=
XM_017013794.1:c.8021C=	XP_016869283.1:p.Ser2674=
XM_017013795.1:c.7985C=	XP_016869284.1:p.Ser2662=
XM_017013796.1:c.7937C=	XP_016869285.1:p.Ser2646=
XM_017013797.1:c.7895C=	XP_016869286.1:p.Ser2632=
NM_003235.5:c.8156C= MANE Select	NP_003226.4:p.Ser2719=