Canonical Allele Identifier: CA1821104905

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133517C= , CM000670.2:g.133133517C=	GRCh38
NC_000008.10:g.134145761C= , CM000670.1:g.134145761C=	GRCh37
NC_000008.9:g.134214943C=	NCBI36
NG_015832.1:g.271557C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8045C= MANE Select	ENSP00000220616.4:p.Ala2682=
ENST00000220616.8:c.8045C=	ENSP00000220616.4:p.Ala2682=
ENST00000519178.5:c.3411C=
ENST00000519543.5:c.2444C=	ENSP00000430430.1:p.Ala815=
ENST00000521107.1:c.257C=	ENSP00000430161.1:p.Ala86=
ENST00000522691.1:n.131C=
ENST00000523756.5:c.4700C=
NM_003235.4:c.8045C=	NP_003226.4:p.Ala2682=
XM_005251038.3:c.7853C=	XP_005251095.1:p.Ala2618=
XM_006716622.2:c.7982C=	XP_006716685.1:p.Ala2661=
XM_005251038.4:c.7853C=	XP_005251095.1:p.Ala2618=
XM_006716622.3:c.7982C=	XP_006716685.1:p.Ala2661=
XM_017013793.1:c.7979C=	XP_016869282.1:p.Ala2660=
XM_017013794.1:c.7910C=	XP_016869283.1:p.Ala2637=
XM_017013795.1:c.7874C=	XP_016869284.1:p.Ala2625=
XM_017013796.1:c.7826C=	XP_016869285.1:p.Ala2609=
XM_017013797.1:c.7784C=	XP_016869286.1:p.Ala2595=
NM_003235.5:c.8045C= MANE Select	NP_003226.4:p.Ala2682=