Canonical Allele Identifier: CA2688653573

Gene: TG

Linked Data

• gnomAD v4: 8-132971718-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132971718C>A , CM000670.2:g.132971718C>A	GRCh38
NC_000008.10:g.133983963C>A , CM000670.1:g.133983963C>A	GRCh37
NC_000008.9:g.134053145C>A	NCBI36
NG_015832.1:g.109759C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.5976-76C>A MANE Select	ENSP00000220616.4:n.5976-76C>A
ENST00000220616.8:c.5976-76C>A	ENSP00000220616.4:n.5976-76C>A
ENST00000519178.5:c.1342-76C>A
ENST00000519543.5:c.438-76C>A	ENSP00000430430.1:n.438-76C>A
ENST00000520089.5:n.85-76C>A
ENST00000520197.5:n.113-76C>A
ENST00000523756.5:c.2631-76C>A
NM_003235.4:c.5976-76C>A	NP_003226.4:n.5976-76C>A
XM_005251038.3:c.5784-76C>A	XP_005251095.1:n.5784-76C>A
XM_005251040.3:c.5976-76C>A	XP_005251097.1:n.5976-76C>A
XM_005251042.3:c.5976-76C>A	XP_005251099.1:n.5976-76C>A
XM_005251043.3:c.5976-76C>A	XP_005251100.1:n.5976-76C>A
XM_006716622.2:c.5976-76C>A	XP_006716685.1:n.5976-76C>A
XM_005251038.4:c.5784-76C>A	XP_005251095.1:n.5784-76C>A
XM_005251040.4:c.5976-76C>A	XP_005251097.1:n.5976-76C>A
XM_005251042.4:c.5976-76C>A	XP_005251099.1:n.5976-76C>A
XM_006716622.3:c.5976-76C>A	XP_006716685.1:n.5976-76C>A
XM_017013793.1:c.5910-76C>A	XP_016869282.1:n.5910-76C>A
XM_017013794.1:c.5976-76C>A	XP_016869283.1:n.5976-76C>A
XM_017013795.1:c.5805-76C>A	XP_016869284.1:n.5805-76C>A
XM_017013796.1:c.5757-76C>A	XP_016869285.1:n.5757-76C>A
XM_017013797.1:c.5715-76C>A	XP_016869286.1:n.5715-76C>A
XM_017013798.1:c.5976-76C>A	XP_016869287.1:n.5976-76C>A
XM_017013799.1:c.5976-76C>A	XP_016869288.1:n.5976-76C>A
XM_017013800.1:c.5976-76C>A	XP_016869289.1:n.5976-76C>A
NM_003235.5:c.5976-76C>A MANE Select	NP_003226.4:n.5976-76C>A