Canonical Allele Identifier: CA372253485

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145845T>A (hg19) ; chr8:g.133133601T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133601T>A , CM000670.2:g.133133601T>A	GRCh38
NC_000008.10:g.134145845T>A , CM000670.1:g.134145845T>A	GRCh37
NC_000008.9:g.134215027T>A	NCBI36
NG_015832.1:g.271641T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8129T>A MANE Select	ENSP00000220616.4:p.Leu2710Gln
ENST00000220616.8:c.8129T>A	ENSP00000220616.4:p.Leu2710Gln
ENST00000519178.5:c.3495T>A
ENST00000519543.5:c.2528T>A	ENSP00000430430.1:p.Leu843Gln
ENST00000521107.1:c.341T>A	ENSP00000430161.1:p.Leu114Gln
ENST00000522691.1:n.215T>A
ENST00000523756.5:c.4784T>A
NM_003235.4:c.8129T>A	NP_003226.4:p.Leu2710Gln
XM_005251038.3:c.7937T>A	XP_005251095.1:p.Leu2646Gln
XM_006716622.2:c.8066T>A	XP_006716685.1:p.Leu2689Gln
XM_005251038.4:c.7937T>A	XP_005251095.1:p.Leu2646Gln
XM_006716622.3:c.8066T>A	XP_006716685.1:p.Leu2689Gln
XM_017013793.1:c.8063T>A	XP_016869282.1:p.Leu2688Gln
XM_017013794.1:c.7994T>A	XP_016869283.1:p.Leu2665Gln
XM_017013795.1:c.7958T>A	XP_016869284.1:p.Leu2653Gln
XM_017013796.1:c.7910T>A	XP_016869285.1:p.Leu2637Gln
XM_017013797.1:c.7868T>A	XP_016869286.1:p.Leu2623Gln
NM_003235.5:c.8129T>A MANE Select	NP_003226.4:p.Leu2710Gln