Canonical Allele Identifier: CA372253093

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145746A>T (hg19) ; chr8:g.133133502A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133502A>T , CM000670.2:g.133133502A>T	GRCh38
NC_000008.10:g.134145746A>T , CM000670.1:g.134145746A>T	GRCh37
NC_000008.9:g.134214928A>T	NCBI36
NG_015832.1:g.271542A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8030A>T MANE Select	ENSP00000220616.4:p.Lys2677Ile
ENST00000220616.8:c.8030A>T	ENSP00000220616.4:p.Lys2677Ile
ENST00000519178.5:c.3396A>T
ENST00000519543.5:c.2429A>T	ENSP00000430430.1:p.Lys810Ile
ENST00000521107.1:c.242A>T	ENSP00000430161.1:p.Lys81Ile
ENST00000522691.1:n.116A>T
ENST00000523756.5:c.4685A>T
NM_003235.4:c.8030A>T	NP_003226.4:p.Lys2677Ile
XM_005251038.3:c.7838A>T	XP_005251095.1:p.Lys2613Ile
XM_006716622.2:c.7967A>T	XP_006716685.1:p.Lys2656Ile
XM_005251038.4:c.7838A>T	XP_005251095.1:p.Lys2613Ile
XM_006716622.3:c.7967A>T	XP_006716685.1:p.Lys2656Ile
XM_017013793.1:c.7964A>T	XP_016869282.1:p.Lys2655Ile
XM_017013794.1:c.7895A>T	XP_016869283.1:p.Lys2632Ile
XM_017013795.1:c.7859A>T	XP_016869284.1:p.Lys2620Ile
XM_017013796.1:c.7811A>T	XP_016869285.1:p.Lys2604Ile
XM_017013797.1:c.7769A>T	XP_016869286.1:p.Lys2590Ile
NM_003235.5:c.8030A>T MANE Select	NP_003226.4:p.Lys2677Ile