Canonical Allele Identifier: CA2688648161

Gene: TG

Linked Data

• gnomAD v4: 8-132873359-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132873359_132873360insA , CM000670.2:g.132873359_132873360insA	GRCh38
NC_000008.10:g.133885604_133885605insA , CM000670.1:g.133885604_133885605insA	GRCh37
NC_000008.9:g.133954786_133954787insA	NCBI36
NG_015832.1:g.11400_11401insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.638+138_638+139insA MANE Select	ENSP00000220616.4:n.638+138_638+139insA
ENST00000220616.8:c.638+138_638+139insA	ENSP00000220616.4:n.638+138_638+139insA
ENST00000523901.1:c.*489+138_*489+139insA	ENSP00000427871.1:n.*489+138_*489+139insA
NM_003235.4:c.638+138_638+139insA	NP_003226.4:n.638+138_638+139insA
XM_005251038.3:c.638+138_638+139insA	XP_005251095.1:n.638+138_638+139insA
XM_005251040.3:c.638+138_638+139insA	XP_005251097.1:n.638+138_638+139insA
XM_005251042.3:c.638+138_638+139insA	XP_005251099.1:n.638+138_638+139insA
XM_005251043.3:c.638+138_638+139insA	XP_005251100.1:n.638+138_638+139insA
XM_006716622.2:c.638+138_638+139insA	XP_006716685.1:n.638+138_638+139insA
XM_005251038.4:c.638+138_638+139insA	XP_005251095.1:n.638+138_638+139insA
XM_005251040.4:c.638+138_638+139insA	XP_005251097.1:n.638+138_638+139insA
XM_005251042.4:c.638+138_638+139insA	XP_005251099.1:n.638+138_638+139insA
XM_006716622.3:c.638+138_638+139insA	XP_006716685.1:n.638+138_638+139insA
XM_017013793.1:c.638+138_638+139insA	XP_016869282.1:n.638+138_638+139insA
XM_017013794.1:c.638+138_638+139insA	XP_016869283.1:n.638+138_638+139insA
XM_017013795.1:c.638+138_638+139insA	XP_016869284.1:n.638+138_638+139insA
XM_017013796.1:c.638+138_638+139insA	XP_016869285.1:n.638+138_638+139insA
XM_017013797.1:c.377+138_377+139insA	XP_016869286.1:n.377+138_377+139insA
XM_017013798.1:c.638+138_638+139insA	XP_016869287.1:n.638+138_638+139insA
XM_017013799.1:c.638+138_638+139insA	XP_016869288.1:n.638+138_638+139insA
XM_017013800.1:c.638+138_638+139insA	XP_016869289.1:n.638+138_638+139insA
NM_003235.5:c.638+138_638+139insA MANE Select	NP_003226.4:n.638+138_638+139insA