Canonical Allele Identifier: CA372253550

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145861C>A (hg19) ; chr8:g.133133617C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133617C>A , CM000670.2:g.133133617C>A	GRCh38
NC_000008.10:g.134145861C>A , CM000670.1:g.134145861C>A	GRCh37
NC_000008.9:g.134215043C>A	NCBI36
NG_015832.1:g.271657C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8145C>A MANE Select	ENSP00000220616.4:p.Cys2715Ter
ENST00000220616.8:c.8145C>A	ENSP00000220616.4:p.Cys2715Ter
ENST00000519178.5:c.3511C>A
ENST00000519543.5:c.2544C>A	ENSP00000430430.1:p.Cys848Ter
ENST00000521107.1:c.357C>A	ENSP00000430161.1:p.Cys119Ter
ENST00000522691.1:n.231C>A
ENST00000523756.5:c.4800C>A
NM_003235.4:c.8145C>A	NP_003226.4:p.Cys2715Ter
XM_005251038.3:c.7953C>A	XP_005251095.1:p.Cys2651Ter
XM_006716622.2:c.8082C>A	XP_006716685.1:p.Cys2694Ter
XM_005251038.4:c.7953C>A	XP_005251095.1:p.Cys2651Ter
XM_006716622.3:c.8082C>A	XP_006716685.1:p.Cys2694Ter
XM_017013793.1:c.8079C>A	XP_016869282.1:p.Cys2693Ter
XM_017013794.1:c.8010C>A	XP_016869283.1:p.Cys2670Ter
XM_017013795.1:c.7974C>A	XP_016869284.1:p.Cys2658Ter
XM_017013796.1:c.7926C>A	XP_016869285.1:p.Cys2642Ter
XM_017013797.1:c.7884C>A	XP_016869286.1:p.Cys2628Ter
NM_003235.5:c.8145C>A MANE Select	NP_003226.4:p.Cys2715Ter