Canonical Allele Identifier: CA372253497

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145848A>T (hg19) ; chr8:g.133133604A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133604A>T , CM000670.2:g.133133604A>T	GRCh38
NC_000008.10:g.134145848A>T , CM000670.1:g.134145848A>T	GRCh37
NC_000008.9:g.134215030A>T	NCBI36
NG_015832.1:g.271644A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8132A>T MANE Select	ENSP00000220616.4:p.Lys2711Met
ENST00000220616.8:c.8132A>T	ENSP00000220616.4:p.Lys2711Met
ENST00000519178.5:c.3498A>T
ENST00000519543.5:c.2531A>T	ENSP00000430430.1:p.Lys844Met
ENST00000521107.1:c.344A>T	ENSP00000430161.1:p.Lys115Met
ENST00000522691.1:n.218A>T
ENST00000523756.5:c.4787A>T
NM_003235.4:c.8132A>T	NP_003226.4:p.Lys2711Met
XM_005251038.3:c.7940A>T	XP_005251095.1:p.Lys2647Met
XM_006716622.2:c.8069A>T	XP_006716685.1:p.Lys2690Met
XM_005251038.4:c.7940A>T	XP_005251095.1:p.Lys2647Met
XM_006716622.3:c.8069A>T	XP_006716685.1:p.Lys2690Met
XM_017013793.1:c.8066A>T	XP_016869282.1:p.Lys2689Met
XM_017013794.1:c.7997A>T	XP_016869283.1:p.Lys2666Met
XM_017013795.1:c.7961A>T	XP_016869284.1:p.Lys2654Met
XM_017013796.1:c.7913A>T	XP_016869285.1:p.Lys2638Met
XM_017013797.1:c.7871A>T	XP_016869286.1:p.Lys2624Met
NM_003235.5:c.8132A>T MANE Select	NP_003226.4:p.Lys2711Met