Canonical Allele Identifier: CA372253623

Gene: TG

Linked Data

• COSMIC: COSM3318430
• MyVariant Identifiers: chr8:g.134145876G>T (hg19) ; chr8:g.133133632G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133632G>T , CM000670.2:g.133133632G>T	GRCh38
NC_000008.10:g.134145876G>T , CM000670.1:g.134145876G>T	GRCh37
NC_000008.9:g.134215058G>T	NCBI36
NG_015832.1:g.271672G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8160G>T MANE Select	ENSP00000220616.4:p.Lys2720Asn
ENST00000220616.8:c.8160G>T	ENSP00000220616.4:p.Lys2720Asn
ENST00000519178.5:c.3526G>T
ENST00000519543.5:c.2559G>T	ENSP00000430430.1:p.Lys853Asn
ENST00000521107.1:c.372G>T	ENSP00000430161.1:p.Lys124Asn
ENST00000522691.1:n.246G>T
ENST00000523756.5:c.4815G>T
NM_003235.4:c.8160G>T	NP_003226.4:p.Lys2720Asn
XM_005251038.3:c.7968G>T	XP_005251095.1:p.Lys2656Asn
XM_006716622.2:c.8097G>T	XP_006716685.1:p.Lys2699Asn
XM_005251038.4:c.7968G>T	XP_005251095.1:p.Lys2656Asn
XM_006716622.3:c.8097G>T	XP_006716685.1:p.Lys2699Asn
XM_017013793.1:c.8094G>T	XP_016869282.1:p.Lys2698Asn
XM_017013794.1:c.8025G>T	XP_016869283.1:p.Lys2675Asn
XM_017013795.1:c.7989G>T	XP_016869284.1:p.Lys2663Asn
XM_017013796.1:c.7941G>T	XP_016869285.1:p.Lys2647Asn
XM_017013797.1:c.7899G>T	XP_016869286.1:p.Lys2633Asn
NM_003235.5:c.8160G>T MANE Select	NP_003226.4:p.Lys2720Asn