Canonical Allele Identifier: CA1821000844

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132967797G= , CM000670.2:g.132967797G=	GRCh38
NC_000008.10:g.133980042G= , CM000670.1:g.133980042G=	GRCh37
NC_000008.9:g.134049224G=	NCBI36
NG_015832.1:g.105838G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.5690G= MANE Select	ENSP00000220616.4:p.Cys1897=
ENST00000220616.8:c.5690G=	ENSP00000220616.4:p.Cys1897=
ENST00000518058.1:c.85G=
ENST00000519178.5:c.1056G=
ENST00000519543.5:c.152G=	ENSP00000430430.1:p.Cys51=
ENST00000523756.5:c.2345G=
NM_003235.4:c.5690G=	NP_003226.4:p.Cys1897=
XM_005251038.3:c.5498G=	XP_005251095.1:p.Cys1833=
XM_005251040.3:c.5690G=	XP_005251097.1:p.Cys1897=
XM_005251042.3:c.5690G=	XP_005251099.1:p.Cys1897=
XM_005251043.3:c.5690G=	XP_005251100.1:p.Cys1897=
XM_006716622.2:c.5690G=	XP_006716685.1:p.Cys1897=
XM_005251038.4:c.5498G=	XP_005251095.1:p.Cys1833=
XM_005251040.4:c.5690G=	XP_005251097.1:p.Cys1897=
XM_005251042.4:c.5690G=	XP_005251099.1:p.Cys1897=
XM_006716622.3:c.5690G=	XP_006716685.1:p.Cys1897=
XM_017013793.1:c.5624G=	XP_016869282.1:p.Cys1875=
XM_017013794.1:c.5690G=	XP_016869283.1:p.Cys1897=
XM_017013795.1:c.5519G=	XP_016869284.1:p.Cys1840=
XM_017013796.1:c.5471G=	XP_016869285.1:p.Cys1824=
XM_017013797.1:c.5429G=	XP_016869286.1:p.Cys1810=
XM_017013798.1:c.5690G=	XP_016869287.1:p.Cys1897=
XM_017013799.1:c.5690G=	XP_016869288.1:p.Cys1897=
XM_017013800.1:c.5690G=	XP_016869289.1:p.Cys1897=
NM_003235.5:c.5690G= MANE Select	NP_003226.4:p.Cys1897=