Canonical Allele Identifier: CA372236544

Gene: TG

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132971805G>C , CM000670.2:g.132971805G>C	GRCh38
NC_000008.10:g.133984050G>C , CM000670.1:g.133984050G>C	GRCh37
NC_000008.9:g.134053232G>C	NCBI36
NG_015832.1:g.109846G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.5987G>C MANE Select	ENSP00000220616.4:p.Cys1996Ser
ENST00000220616.8:c.5987G>C	ENSP00000220616.4:p.Cys1996Ser
ENST00000519178.5:c.1353G>C
ENST00000519543.5:c.449G>C	ENSP00000430430.1:p.Cys150Ser
ENST00000520089.5:n.96G>C
ENST00000520197.5:n.124G>C
ENST00000523756.5:c.2642G>C
NM_003235.4:c.5987G>C	NP_003226.4:p.Cys1996Ser
XM_005251038.3:c.5795G>C	XP_005251095.1:p.Cys1932Ser
XM_005251040.3:c.5987G>C	XP_005251097.1:p.Cys1996Ser
XM_005251042.3:c.5987G>C	XP_005251099.1:p.Cys1996Ser
XM_005251043.3:c.5987G>C	XP_005251100.1:p.Cys1996Ser
XM_006716622.2:c.5987G>C	XP_006716685.1:p.Cys1996Ser
XM_005251038.4:c.5795G>C	XP_005251095.1:p.Cys1932Ser
XM_005251040.4:c.5987G>C	XP_005251097.1:p.Cys1996Ser
XM_005251042.4:c.5987G>C	XP_005251099.1:p.Cys1996Ser
XM_006716622.3:c.5987G>C	XP_006716685.1:p.Cys1996Ser
XM_017013793.1:c.5921G>C	XP_016869282.1:p.Cys1974Ser
XM_017013794.1:c.5987G>C	XP_016869283.1:p.Cys1996Ser
XM_017013795.1:c.5816G>C	XP_016869284.1:p.Cys1939Ser
XM_017013796.1:c.5768G>C	XP_016869285.1:p.Cys1923Ser
XM_017013797.1:c.5726G>C	XP_016869286.1:p.Cys1909Ser
XM_017013798.1:c.5987G>C	XP_016869287.1:p.Cys1996Ser
XM_017013799.1:c.5987G>C	XP_016869288.1:p.Cys1996Ser
XM_017013800.1:c.5987G>C	XP_016869289.1:p.Cys1996Ser
NM_003235.5:c.5987G>C MANE Select	NP_003226.4:p.Cys1996Ser