Canonical Allele Identifier: CA372253257

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145787C>A (hg19) ; chr8:g.133133543C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133543C>A , CM000670.2:g.133133543C>A	GRCh38
NC_000008.10:g.134145787C>A , CM000670.1:g.134145787C>A	GRCh37
NC_000008.9:g.134214969C>A	NCBI36
NG_015832.1:g.271583C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8071C>A MANE Select	ENSP00000220616.4:p.Arg2691Ser
ENST00000220616.8:c.8071C>A	ENSP00000220616.4:p.Arg2691Ser
ENST00000519178.5:c.3437C>A
ENST00000519543.5:c.2470C>A	ENSP00000430430.1:p.Arg824Ser
ENST00000521107.1:c.283C>A	ENSP00000430161.1:p.Arg95Ser
ENST00000522691.1:n.157C>A
ENST00000523756.5:c.4726C>A
NM_003235.4:c.8071C>A	NP_003226.4:p.Arg2691Ser
XM_005251038.3:c.7879C>A	XP_005251095.1:p.Arg2627Ser
XM_006716622.2:c.8008C>A	XP_006716685.1:p.Arg2670Ser
XM_005251038.4:c.7879C>A	XP_005251095.1:p.Arg2627Ser
XM_006716622.3:c.8008C>A	XP_006716685.1:p.Arg2670Ser
XM_017013793.1:c.8005C>A	XP_016869282.1:p.Arg2669Ser
XM_017013794.1:c.7936C>A	XP_016869283.1:p.Arg2646Ser
XM_017013795.1:c.7900C>A	XP_016869284.1:p.Arg2634Ser
XM_017013796.1:c.7852C>A	XP_016869285.1:p.Arg2618Ser
XM_017013797.1:c.7810C>A	XP_016869286.1:p.Arg2604Ser
NM_003235.5:c.8071C>A MANE Select	NP_003226.4:p.Arg2691Ser