Canonical Allele Identifier: CA372253023

Gene: TG

Linked Data

• gnomAD v4: 8-133133484-C-T
• MyVariant Identifiers: chr8:g.134145728C>T (hg19) ; chr8:g.133133484C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133484C>T , CM000670.2:g.133133484C>T	GRCh38
NC_000008.10:g.134145728C>T , CM000670.1:g.134145728C>T	GRCh37
NC_000008.9:g.134214910C>T	NCBI36
NG_015832.1:g.271524C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8012C>T MANE Select	ENSP00000220616.4:p.Pro2671Leu
ENST00000220616.8:c.8012C>T	ENSP00000220616.4:p.Pro2671Leu
ENST00000519178.5:c.3378C>T
ENST00000519543.5:c.2411C>T	ENSP00000430430.1:p.Pro804Leu
ENST00000521107.1:c.224C>T	ENSP00000430161.1:p.Pro75Leu
ENST00000522691.1:n.98C>T
ENST00000523756.5:c.4667C>T
NM_003235.4:c.8012C>T	NP_003226.4:p.Pro2671Leu
XM_005251038.3:c.7820C>T	XP_005251095.1:p.Pro2607Leu
XM_006716622.2:c.7949C>T	XP_006716685.1:p.Pro2650Leu
XM_005251038.4:c.7820C>T	XP_005251095.1:p.Pro2607Leu
XM_006716622.3:c.7949C>T	XP_006716685.1:p.Pro2650Leu
XM_017013793.1:c.7946C>T	XP_016869282.1:p.Pro2649Leu
XM_017013794.1:c.7877C>T	XP_016869283.1:p.Pro2626Leu
XM_017013795.1:c.7841C>T	XP_016869284.1:p.Pro2614Leu
XM_017013796.1:c.7793C>T	XP_016869285.1:p.Pro2598Leu
XM_017013797.1:c.7751C>T	XP_016869286.1:p.Pro2584Leu
NM_003235.5:c.8012C>T MANE Select	NP_003226.4:p.Pro2671Leu