Canonical Allele Identifier: CA1821104950

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133596G= , CM000670.2:g.133133596G=	GRCh38
NC_000008.10:g.134145840G= , CM000670.1:g.134145840G=	GRCh37
NC_000008.9:g.134215022G=	NCBI36
NG_015832.1:g.271636G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8124G= MANE Select	ENSP00000220616.4:p.Gln2708=
ENST00000220616.8:c.8124G=	ENSP00000220616.4:p.Gln2708=
ENST00000519178.5:c.3490G=
ENST00000519543.5:c.2523G=	ENSP00000430430.1:p.Gln841=
ENST00000521107.1:c.336G=	ENSP00000430161.1:p.Gln112=
ENST00000522691.1:n.210G=
ENST00000523756.5:c.4779G=
NM_003235.4:c.8124G=	NP_003226.4:p.Gln2708=
XM_005251038.3:c.7932G=	XP_005251095.1:p.Gln2644=
XM_006716622.2:c.8061G=	XP_006716685.1:p.Gln2687=
XM_005251038.4:c.7932G=	XP_005251095.1:p.Gln2644=
XM_006716622.3:c.8061G=	XP_006716685.1:p.Gln2687=
XM_017013793.1:c.8058G=	XP_016869282.1:p.Gln2686=
XM_017013794.1:c.7989G=	XP_016869283.1:p.Gln2663=
XM_017013795.1:c.7953G=	XP_016869284.1:p.Gln2651=
XM_017013796.1:c.7905G=	XP_016869285.1:p.Gln2635=
XM_017013797.1:c.7863G=	XP_016869286.1:p.Gln2621=
NM_003235.5:c.8124G= MANE Select	NP_003226.4:p.Gln2708=