Canonical Allele Identifier: CA1821104949

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133594C= , CM000670.2:g.133133594C=	GRCh38
NC_000008.10:g.134145838C= , CM000670.1:g.134145838C=	GRCh37
NC_000008.9:g.134215020C=	NCBI36
NG_015832.1:g.271634C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8122C= MANE Select	ENSP00000220616.4:p.Gln2708=
ENST00000220616.8:c.8122C=	ENSP00000220616.4:p.Gln2708=
ENST00000519178.5:c.3488C=
ENST00000519543.5:c.2521C=	ENSP00000430430.1:p.Gln841=
ENST00000521107.1:c.334C=	ENSP00000430161.1:p.Gln112=
ENST00000522691.1:n.208C=
ENST00000523756.5:c.4777C=
NM_003235.4:c.8122C=	NP_003226.4:p.Gln2708=
XM_005251038.3:c.7930C=	XP_005251095.1:p.Gln2644=
XM_006716622.2:c.8059C=	XP_006716685.1:p.Gln2687=
XM_005251038.4:c.7930C=	XP_005251095.1:p.Gln2644=
XM_006716622.3:c.8059C=	XP_006716685.1:p.Gln2687=
XM_017013793.1:c.8056C=	XP_016869282.1:p.Gln2686=
XM_017013794.1:c.7987C=	XP_016869283.1:p.Gln2663=
XM_017013795.1:c.7951C=	XP_016869284.1:p.Gln2651=
XM_017013796.1:c.7903C=	XP_016869285.1:p.Gln2635=
XM_017013797.1:c.7861C=	XP_016869286.1:p.Gln2621=
NM_003235.5:c.8122C= MANE Select	NP_003226.4:p.Gln2708=