Canonical Allele Identifier: CA1821104883

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133473T= , CM000670.2:g.133133473T=	GRCh38
NC_000008.10:g.134145717T= , CM000670.1:g.134145717T=	GRCh37
NC_000008.9:g.134214899T=	NCBI36
NG_015832.1:g.271513T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8001T= MANE Select	ENSP00000220616.4:p.Asn2667=
ENST00000220616.8:c.8001T=	ENSP00000220616.4:p.Asn2667=
ENST00000519178.5:c.3367T=
ENST00000519543.5:c.2400T=	ENSP00000430430.1:p.Asn800=
ENST00000521107.1:c.213T=	ENSP00000430161.1:p.Asn71=
ENST00000522691.1:n.87T=
ENST00000523756.5:c.4656T=
NM_003235.4:c.8001T=	NP_003226.4:p.Asn2667=
XM_005251038.3:c.7809T=	XP_005251095.1:p.Asn2603=
XM_006716622.2:c.7938T=	XP_006716685.1:p.Asn2646=
XM_005251038.4:c.7809T=	XP_005251095.1:p.Asn2603=
XM_006716622.3:c.7938T=	XP_006716685.1:p.Asn2646=
XM_017013793.1:c.7935T=	XP_016869282.1:p.Asn2645=
XM_017013794.1:c.7866T=	XP_016869283.1:p.Asn2622=
XM_017013795.1:c.7830T=	XP_016869284.1:p.Asn2610=
XM_017013796.1:c.7782T=	XP_016869285.1:p.Asn2594=
XM_017013797.1:c.7740T=	XP_016869286.1:p.Asn2580=
NM_003235.5:c.8001T= MANE Select	NP_003226.4:p.Asn2667=