Canonical Allele Identifier: CA463013053

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134030204C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017959C>A , CM000670.2:g.133017959C>A	GRCh38
NC_000008.10:g.134030204C>A , CM000670.1:g.134030204C>A	GRCh37
NC_000008.9:g.134099386C>A	NCBI36
NG_015832.1:g.156000C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6744C>A MANE Select	ENSP00000220616.4:p.Pro2248=
ENST00000220616.8:c.6744C>A	ENSP00000220616.4:p.Pro2248=
ENST00000518108.1:c.168+93C>A
ENST00000519178.5:c.2110C>A
ENST00000519543.5:c.1143C>A	ENSP00000430430.1:p.Pro381=
ENST00000522523.5:n.805C>A
ENST00000523756.5:c.3399C>A
NM_003235.4:c.6744C>A	NP_003226.4:p.Pro2248=
XM_005251038.3:c.6552C>A	XP_005251095.1:p.Pro2184=
XM_006716622.2:c.6681C>A	XP_006716685.1:p.Pro2227=
XM_005251038.4:c.6552C>A	XP_005251095.1:p.Pro2184=
XM_006716622.3:c.6681C>A	XP_006716685.1:p.Pro2227=
XM_017013793.1:c.6678C>A	XP_016869282.1:p.Pro2226=
XM_017013794.1:c.6744C>A	XP_016869283.1:p.Pro2248=
XM_017013795.1:c.6573C>A	XP_016869284.1:p.Pro2191=
XM_017013796.1:c.6525C>A	XP_016869285.1:p.Pro2175=
XM_017013797.1:c.6483C>A	XP_016869286.1:p.Pro2161=
XM_017013798.1:c.6744C>A	XP_016869287.1:p.Pro2248=
NM_003235.5:c.6744C>A MANE Select	NP_003226.4:p.Pro2248=