Canonical Allele Identifier: CA372253672

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145889C>A (hg19) ; chr8:g.133133645C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133645C>A , CM000670.2:g.133133645C>A	GRCh38
NC_000008.10:g.134145889C>A , CM000670.1:g.134145889C>A	GRCh37
NC_000008.9:g.134215071C>A	NCBI36
NG_015832.1:g.271685C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8173C>A MANE Select	ENSP00000220616.4:p.Leu2725Met
ENST00000220616.8:c.8173C>A	ENSP00000220616.4:p.Leu2725Met
ENST00000519178.5:c.3539C>A
ENST00000519543.5:c.2572C>A	ENSP00000430430.1:p.Leu858Met
ENST00000521107.1:c.385C>A	ENSP00000430161.1:p.Leu129Met
ENST00000522691.1:n.259C>A
ENST00000523756.5:c.4828C>A
NM_003235.4:c.8173C>A	NP_003226.4:p.Leu2725Met
XM_005251038.3:c.7981C>A	XP_005251095.1:p.Leu2661Met
XM_006716622.2:c.8110C>A	XP_006716685.1:p.Leu2704Met
XM_005251038.4:c.7981C>A	XP_005251095.1:p.Leu2661Met
XM_006716622.3:c.8110C>A	XP_006716685.1:p.Leu2704Met
XM_017013793.1:c.8107C>A	XP_016869282.1:p.Leu2703Met
XM_017013794.1:c.8038C>A	XP_016869283.1:p.Leu2680Met
XM_017013795.1:c.8002C>A	XP_016869284.1:p.Leu2668Met
XM_017013796.1:c.7954C>A	XP_016869285.1:p.Leu2652Met
XM_017013797.1:c.7912C>A	XP_016869286.1:p.Leu2638Met
NM_003235.5:c.8173C>A MANE Select	NP_003226.4:p.Leu2725Met