Canonical Allele Identifier: CA372253202

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145773C>T (hg19) ; chr8:g.133133529C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133529C>T , CM000670.2:g.133133529C>T	GRCh38
NC_000008.10:g.134145773C>T , CM000670.1:g.134145773C>T	GRCh37
NC_000008.9:g.134214955C>T	NCBI36
NG_015832.1:g.271569C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8057C>T MANE Select	ENSP00000220616.4:p.Pro2686Leu
ENST00000220616.8:c.8057C>T	ENSP00000220616.4:p.Pro2686Leu
ENST00000519178.5:c.3423C>T
ENST00000519543.5:c.2456C>T	ENSP00000430430.1:p.Pro819Leu
ENST00000521107.1:c.269C>T	ENSP00000430161.1:p.Pro90Leu
ENST00000522691.1:n.143C>T
ENST00000523756.5:c.4712C>T
NM_003235.4:c.8057C>T	NP_003226.4:p.Pro2686Leu
XM_005251038.3:c.7865C>T	XP_005251095.1:p.Pro2622Leu
XM_006716622.2:c.7994C>T	XP_006716685.1:p.Pro2665Leu
XM_005251038.4:c.7865C>T	XP_005251095.1:p.Pro2622Leu
XM_006716622.3:c.7994C>T	XP_006716685.1:p.Pro2665Leu
XM_017013793.1:c.7991C>T	XP_016869282.1:p.Pro2664Leu
XM_017013794.1:c.7922C>T	XP_016869283.1:p.Pro2641Leu
XM_017013795.1:c.7886C>T	XP_016869284.1:p.Pro2629Leu
XM_017013796.1:c.7838C>T	XP_016869285.1:p.Pro2613Leu
XM_017013797.1:c.7796C>T	XP_016869286.1:p.Pro2599Leu
NM_003235.5:c.8057C>T MANE Select	NP_003226.4:p.Pro2686Leu