Canonical Allele Identifier: CA372253270

Gene: TG

Linked Data

• COSMIC: COSM1229065
• MyVariant Identifiers: chr8:g.134145791C>A (hg19) ; chr8:g.133133547C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133547C>A , CM000670.2:g.133133547C>A	GRCh38
NC_000008.10:g.134145791C>A , CM000670.1:g.134145791C>A	GRCh37
NC_000008.9:g.134214973C>A	NCBI36
NG_015832.1:g.271587C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8075C>A MANE Select	ENSP00000220616.4:p.Ala2692Asp
ENST00000220616.8:c.8075C>A	ENSP00000220616.4:p.Ala2692Asp
ENST00000519178.5:c.3441C>A
ENST00000519543.5:c.2474C>A	ENSP00000430430.1:p.Ala825Asp
ENST00000521107.1:c.287C>A	ENSP00000430161.1:p.Ala96Asp
ENST00000522691.1:n.161C>A
ENST00000523756.5:c.4730C>A
NM_003235.4:c.8075C>A	NP_003226.4:p.Ala2692Asp
XM_005251038.3:c.7883C>A	XP_005251095.1:p.Ala2628Asp
XM_006716622.2:c.8012C>A	XP_006716685.1:p.Ala2671Asp
XM_005251038.4:c.7883C>A	XP_005251095.1:p.Ala2628Asp
XM_006716622.3:c.8012C>A	XP_006716685.1:p.Ala2671Asp
XM_017013793.1:c.8009C>A	XP_016869282.1:p.Ala2670Asp
XM_017013794.1:c.7940C>A	XP_016869283.1:p.Ala2647Asp
XM_017013795.1:c.7904C>A	XP_016869284.1:p.Ala2635Asp
XM_017013796.1:c.7856C>A	XP_016869285.1:p.Ala2619Asp
XM_017013797.1:c.7814C>A	XP_016869286.1:p.Ala2605Asp
NM_003235.5:c.8075C>A MANE Select	NP_003226.4:p.Ala2692Asp