Canonical Allele Identifier: CA372253488

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145847A>C (hg19) ; chr8:g.133133603A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133603A>C , CM000670.2:g.133133603A>C	GRCh38
NC_000008.10:g.134145847A>C , CM000670.1:g.134145847A>C	GRCh37
NC_000008.9:g.134215029A>C	NCBI36
NG_015832.1:g.271643A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8131A>C MANE Select	ENSP00000220616.4:p.Lys2711Gln
ENST00000220616.8:c.8131A>C	ENSP00000220616.4:p.Lys2711Gln
ENST00000519178.5:c.3497A>C
ENST00000519543.5:c.2530A>C	ENSP00000430430.1:p.Lys844Gln
ENST00000521107.1:c.343A>C	ENSP00000430161.1:p.Lys115Gln
ENST00000522691.1:n.217A>C
ENST00000523756.5:c.4786A>C
NM_003235.4:c.8131A>C	NP_003226.4:p.Lys2711Gln
XM_005251038.3:c.7939A>C	XP_005251095.1:p.Lys2647Gln
XM_006716622.2:c.8068A>C	XP_006716685.1:p.Lys2690Gln
XM_005251038.4:c.7939A>C	XP_005251095.1:p.Lys2647Gln
XM_006716622.3:c.8068A>C	XP_006716685.1:p.Lys2690Gln
XM_017013793.1:c.8065A>C	XP_016869282.1:p.Lys2689Gln
XM_017013794.1:c.7996A>C	XP_016869283.1:p.Lys2666Gln
XM_017013795.1:c.7960A>C	XP_016869284.1:p.Lys2654Gln
XM_017013796.1:c.7912A>C	XP_016869285.1:p.Lys2638Gln
XM_017013797.1:c.7870A>C	XP_016869286.1:p.Lys2624Gln
NM_003235.5:c.8131A>C MANE Select	NP_003226.4:p.Lys2711Gln