Canonical Allele Identifier: CA2688656434

Gene: TG

Linked Data

• gnomAD v4: 8-133017998-G-GGCCAGC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017998_133017999insGCCAGC , CM000670.2:g.133017998_133017999insGCCAGC	GRCh38
NC_000008.10:g.134030243_134030244insGCCAGC , CM000670.1:g.134030243_134030244insGCCAGC	GRCh37
NC_000008.9:g.134099425_134099426insGCCAGC	NCBI36
NG_015832.1:g.156039_156040insGCCAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6782+1_6782+2insGCCAGC MANE Select	ENSP00000220616.4:n.6782+1_6782+2insGCCAGC
ENST00000220616.8:c.6782+1_6782+2insGCCAGC	ENSP00000220616.4:n.6782+1_6782+2insGCCAGC
ENST00000518108.1:c.168+132_168+133insGCCAGC
ENST00000519178.5:c.2148+1_2148+2insGCCAGC
ENST00000519543.5:c.1181+1_1181+2insGCCAGC	ENSP00000430430.1:n.1181+1_1181+2insGCCAGC
ENST00000523756.5:c.3437+1_3437+2insGCCAGC
NM_003235.4:c.6782+1_6782+2insGCCAGC	NP_003226.4:n.6782+1_6782+2insGCCAGC
XM_005251038.3:c.6590+1_6590+2insGCCAGC	XP_005251095.1:n.6590+1_6590+2insGCCAGC
XM_006716622.2:c.6719+1_6719+2insGCCAGC	XP_006716685.1:n.6719+1_6719+2insGCCAGC
XM_005251038.4:c.6590+1_6590+2insGCCAGC	XP_005251095.1:n.6590+1_6590+2insGCCAGC
XM_006716622.3:c.6719+1_6719+2insGCCAGC	XP_006716685.1:n.6719+1_6719+2insGCCAGC
XM_017013793.1:c.6716+1_6716+2insGCCAGC	XP_016869282.1:n.6716+1_6716+2insGCCAGC
XM_017013794.1:c.6782+1_6782+2insGCCAGC	XP_016869283.1:n.6782+1_6782+2insGCCAGC
XM_017013795.1:c.6611+1_6611+2insGCCAGC	XP_016869284.1:n.6611+1_6611+2insGCCAGC
XM_017013796.1:c.6563+1_6563+2insGCCAGC	XP_016869285.1:n.6563+1_6563+2insGCCAGC
XM_017013797.1:c.6521+1_6521+2insGCCAGC	XP_016869286.1:n.6521+1_6521+2insGCCAGC
XM_017013798.1:c.6782+1_6782+2insGCCAGC	XP_016869287.1:n.6782+1_6782+2insGCCAGC
NM_003235.5:c.6782+1_6782+2insGCCAGC MANE Select	NP_003226.4:n.6782+1_6782+2insGCCAGC