Canonical Allele Identifier: CA372253456

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145838C>A (hg19) ; chr8:g.133133594C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133594C>A , CM000670.2:g.133133594C>A	GRCh38
NC_000008.10:g.134145838C>A , CM000670.1:g.134145838C>A	GRCh37
NC_000008.9:g.134215020C>A	NCBI36
NG_015832.1:g.271634C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8122C>A MANE Select	ENSP00000220616.4:p.Gln2708Lys
ENST00000220616.8:c.8122C>A	ENSP00000220616.4:p.Gln2708Lys
ENST00000519178.5:c.3488C>A
ENST00000519543.5:c.2521C>A	ENSP00000430430.1:p.Gln841Lys
ENST00000521107.1:c.334C>A	ENSP00000430161.1:p.Gln112Lys
ENST00000522691.1:n.208C>A
ENST00000523756.5:c.4777C>A
NM_003235.4:c.8122C>A	NP_003226.4:p.Gln2708Lys
XM_005251038.3:c.7930C>A	XP_005251095.1:p.Gln2644Lys
XM_006716622.2:c.8059C>A	XP_006716685.1:p.Gln2687Lys
XM_005251038.4:c.7930C>A	XP_005251095.1:p.Gln2644Lys
XM_006716622.3:c.8059C>A	XP_006716685.1:p.Gln2687Lys
XM_017013793.1:c.8056C>A	XP_016869282.1:p.Gln2686Lys
XM_017013794.1:c.7987C>A	XP_016869283.1:p.Gln2663Lys
XM_017013795.1:c.7951C>A	XP_016869284.1:p.Gln2651Lys
XM_017013796.1:c.7903C>A	XP_016869285.1:p.Gln2635Lys
XM_017013797.1:c.7861C>A	XP_016869286.1:p.Gln2621Lys
NM_003235.5:c.8122C>A MANE Select	NP_003226.4:p.Gln2708Lys