Canonical Allele Identifier: CA372253677

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145890T>C (hg19) ; chr8:g.133133646T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133646T>C , CM000670.2:g.133133646T>C	GRCh38
NC_000008.10:g.134145890T>C , CM000670.1:g.134145890T>C	GRCh37
NC_000008.9:g.134215072T>C	NCBI36
NG_015832.1:g.271686T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8174T>C MANE Select	ENSP00000220616.4:p.Leu2725Pro
ENST00000220616.8:c.8174T>C	ENSP00000220616.4:p.Leu2725Pro
ENST00000519178.5:c.3540T>C
ENST00000519543.5:c.2573T>C	ENSP00000430430.1:p.Leu858Pro
ENST00000521107.1:c.386T>C	ENSP00000430161.1:p.Leu129Pro
ENST00000522691.1:n.260T>C
ENST00000523756.5:c.4829T>C
NM_003235.4:c.8174T>C	NP_003226.4:p.Leu2725Pro
XM_005251038.3:c.7982T>C	XP_005251095.1:p.Leu2661Pro
XM_006716622.2:c.8111T>C	XP_006716685.1:p.Leu2704Pro
XM_005251038.4:c.7982T>C	XP_005251095.1:p.Leu2661Pro
XM_006716622.3:c.8111T>C	XP_006716685.1:p.Leu2704Pro
XM_017013793.1:c.8108T>C	XP_016869282.1:p.Leu2703Pro
XM_017013794.1:c.8039T>C	XP_016869283.1:p.Leu2680Pro
XM_017013795.1:c.8003T>C	XP_016869284.1:p.Leu2668Pro
XM_017013796.1:c.7955T>C	XP_016869285.1:p.Leu2652Pro
XM_017013797.1:c.7913T>C	XP_016869286.1:p.Leu2638Pro
NM_003235.5:c.8174T>C MANE Select	NP_003226.4:p.Leu2725Pro