Canonical Allele Identifier: CA372253525

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145854C>T (hg19) ; chr8:g.133133610C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133610C>T , CM000670.2:g.133133610C>T	GRCh38
NC_000008.10:g.134145854C>T , CM000670.1:g.134145854C>T	GRCh37
NC_000008.9:g.134215036C>T	NCBI36
NG_015832.1:g.271650C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8138C>T MANE Select	ENSP00000220616.4:p.Ala2713Val
ENST00000220616.8:c.8138C>T	ENSP00000220616.4:p.Ala2713Val
ENST00000519178.5:c.3504C>T
ENST00000519543.5:c.2537C>T	ENSP00000430430.1:p.Ala846Val
ENST00000521107.1:c.350C>T	ENSP00000430161.1:p.Ala117Val
ENST00000522691.1:n.224C>T
ENST00000523756.5:c.4793C>T
NM_003235.4:c.8138C>T	NP_003226.4:p.Ala2713Val
XM_005251038.3:c.7946C>T	XP_005251095.1:p.Ala2649Val
XM_006716622.2:c.8075C>T	XP_006716685.1:p.Ala2692Val
XM_005251038.4:c.7946C>T	XP_005251095.1:p.Ala2649Val
XM_006716622.3:c.8075C>T	XP_006716685.1:p.Ala2692Val
XM_017013793.1:c.8072C>T	XP_016869282.1:p.Ala2691Val
XM_017013794.1:c.8003C>T	XP_016869283.1:p.Ala2668Val
XM_017013795.1:c.7967C>T	XP_016869284.1:p.Ala2656Val
XM_017013796.1:c.7919C>T	XP_016869285.1:p.Ala2640Val
XM_017013797.1:c.7877C>T	XP_016869286.1:p.Ala2626Val
NM_003235.5:c.8138C>T MANE Select	NP_003226.4:p.Ala2713Val