Canonical Allele Identifier: CA4883690

Gene: TG

Linked Data

• dbSNP Id: rs772415863
• ExAC: 8:133911065 TCG / T
• gnomAD v2: 8-133911065-TCG-T
• gnomAD v3: 8-132898820-TCG-T
• gnomAD v4: 8-132898820-TCG-T
• MyVariant Identifiers: chr8:g.133911066_133911067del (hg19) ; chr8:g.132898821_132898822del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132898821_132898822del , CM000670.2:g.132898821_132898822del	GRCh38
NC_000008.10:g.133911066_133911067del , CM000670.1:g.133911066_133911067del	GRCh37
NC_000008.9:g.133980248_133980249del	NCBI36
NG_015832.1:g.36862_36863del

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.3241_3242del MANE Select	ENSP00000220616.4:p.Arg1081AsnfsTer12
ENST00000220616.8:c.3241_3242del	ENSP00000220616.4:p.Arg1081AsnfsTer12
ENST00000518097.1:n.155_156del
ENST00000518505.1:c.141_142del
ENST00000523756.5:c.200_201del
NM_003235.4:c.3241_3242del	NP_003226.4:p.Arg1081AsnfsTer12
XM_005251038.3:c.3241_3242del	XP_005251095.1:p.Arg1081AsnfsTer12
XM_005251040.3:c.3241_3242del	XP_005251097.1:p.Arg1081AsnfsTer12
XM_005251042.3:c.3241_3242del	XP_005251099.1:p.Arg1081AsnfsTer12
XM_005251043.3:c.3241_3242del	XP_005251100.1:p.Arg1081AsnfsTer12
XM_006716622.2:c.3241_3242del	XP_006716685.1:p.Arg1081AsnfsTer12
XM_005251038.4:c.3241_3242del	XP_005251095.1:p.Arg1081AsnfsTer12
XM_005251040.4:c.3241_3242del	XP_005251097.1:p.Arg1081AsnfsTer12
XM_005251042.4:c.3241_3242del	XP_005251099.1:p.Arg1081AsnfsTer12
XM_006716622.3:c.3241_3242del	XP_006716685.1:p.Arg1081AsnfsTer12
XM_017013793.1:c.3241_3242del	XP_016869282.1:p.Arg1081AsnfsTer12
XM_017013794.1:c.3241_3242del	XP_016869283.1:p.Arg1081AsnfsTer12
XM_017013795.1:c.3241_3242del	XP_016869284.1:p.Arg1081AsnfsTer12
XM_017013796.1:c.3241_3242del	XP_016869285.1:p.Arg1081AsnfsTer12
XM_017013797.1:c.2980_2981del	XP_016869286.1:p.Arg994AsnfsTer12
XM_017013798.1:c.3241_3242del	XP_016869287.1:p.Arg1081AsnfsTer12
XM_017013799.1:c.3241_3242del	XP_016869288.1:p.Arg1081AsnfsTer12
XM_017013800.1:c.3241_3242del	XP_016869289.1:p.Arg1081AsnfsTer12
NM_003235.5:c.3241_3242del MANE Select	NP_003226.4:p.Arg1081AsnfsTer12