Canonical Allele Identifier: CA463016983

Gene: TG

Linked Data

• gnomAD v4: 8-133133476-C-A
• MyVariant Identifiers: chr8:g.134145720C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133476C>A , CM000670.2:g.133133476C>A	GRCh38
NC_000008.10:g.134145720C>A , CM000670.1:g.134145720C>A	GRCh37
NC_000008.9:g.134214902C>A	NCBI36
NG_015832.1:g.271516C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8004C>A MANE Select	ENSP00000220616.4:p.Pro2668=
ENST00000220616.8:c.8004C>A	ENSP00000220616.4:p.Pro2668=
ENST00000519178.5:c.3370C>A
ENST00000519543.5:c.2403C>A	ENSP00000430430.1:p.Pro801=
ENST00000521107.1:c.216C>A	ENSP00000430161.1:p.Pro72=
ENST00000522691.1:n.90C>A
ENST00000523756.5:c.4659C>A
NM_003235.4:c.8004C>A	NP_003226.4:p.Pro2668=
XM_005251038.3:c.7812C>A	XP_005251095.1:p.Pro2604=
XM_006716622.2:c.7941C>A	XP_006716685.1:p.Pro2647=
XM_005251038.4:c.7812C>A	XP_005251095.1:p.Pro2604=
XM_006716622.3:c.7941C>A	XP_006716685.1:p.Pro2647=
XM_017013793.1:c.7938C>A	XP_016869282.1:p.Pro2646=
XM_017013794.1:c.7869C>A	XP_016869283.1:p.Pro2623=
XM_017013795.1:c.7833C>A	XP_016869284.1:p.Pro2611=
XM_017013796.1:c.7785C>A	XP_016869285.1:p.Pro2595=
XM_017013797.1:c.7743C>A	XP_016869286.1:p.Pro2581=
NM_003235.5:c.8004C>A MANE Select	NP_003226.4:p.Pro2668=