Canonical Allele Identifier: CA372253498

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145849G>C (hg19) ; chr8:g.133133605G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133605G>C , CM000670.2:g.133133605G>C	GRCh38
NC_000008.10:g.134145849G>C , CM000670.1:g.134145849G>C	GRCh37
NC_000008.9:g.134215031G>C	NCBI36
NG_015832.1:g.271645G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8133G>C MANE Select	ENSP00000220616.4:p.Lys2711Asn
ENST00000220616.8:c.8133G>C	ENSP00000220616.4:p.Lys2711Asn
ENST00000519178.5:c.3499G>C
ENST00000519543.5:c.2532G>C	ENSP00000430430.1:p.Lys844Asn
ENST00000521107.1:c.345G>C	ENSP00000430161.1:p.Lys115Asn
ENST00000522691.1:n.219G>C
ENST00000523756.5:c.4788G>C
NM_003235.4:c.8133G>C	NP_003226.4:p.Lys2711Asn
XM_005251038.3:c.7941G>C	XP_005251095.1:p.Lys2647Asn
XM_006716622.2:c.8070G>C	XP_006716685.1:p.Lys2690Asn
XM_005251038.4:c.7941G>C	XP_005251095.1:p.Lys2647Asn
XM_006716622.3:c.8070G>C	XP_006716685.1:p.Lys2690Asn
XM_017013793.1:c.8067G>C	XP_016869282.1:p.Lys2689Asn
XM_017013794.1:c.7998G>C	XP_016869283.1:p.Lys2666Asn
XM_017013795.1:c.7962G>C	XP_016869284.1:p.Lys2654Asn
XM_017013796.1:c.7914G>C	XP_016869285.1:p.Lys2638Asn
XM_017013797.1:c.7872G>C	XP_016869286.1:p.Lys2624Asn
NM_003235.5:c.8133G>C MANE Select	NP_003226.4:p.Lys2711Asn