Canonical Allele Identifier: CA2579253657

Gene: TG

Linked Data

• ClinVar Variation Id: 1176276
• ClinVar RCV Id: RCV001531719
• dbSNP Id: rs2132059579

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132873092_132873094del , CM000670.2:g.132873092_132873094del	GRCh38
NC_000008.10:g.133885337_133885339del , CM000670.1:g.133885337_133885339del	GRCh37
NC_000008.9:g.133954519_133954521del	NCBI36
NG_015832.1:g.11133_11135del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.509_511del MANE Select	ENSP00000220616.4:p.Arg170del
ENST00000220616.8:c.509_511del	ENSP00000220616.4:p.Arg170del
ENST00000523901.1:c.*360_*362del	ENSP00000427871.1:n.*360_*362del
NM_003235.4:c.509_511del	NP_003226.4:p.Arg170del
XM_005251038.3:c.509_511del	XP_005251095.1:p.Arg170del
XM_005251040.3:c.509_511del	XP_005251097.1:p.Arg170del
XM_005251042.3:c.509_511del	XP_005251099.1:p.Arg170del
XM_005251043.3:c.509_511del	XP_005251100.1:p.Arg170del
XM_006716622.2:c.509_511del	XP_006716685.1:p.Arg170del
XM_005251038.4:c.509_511del	XP_005251095.1:p.Arg170del
XM_005251040.4:c.509_511del	XP_005251097.1:p.Arg170del
XM_005251042.4:c.509_511del	XP_005251099.1:p.Arg170del
XM_006716622.3:c.509_511del	XP_006716685.1:p.Arg170del
XM_017013793.1:c.509_511del	XP_016869282.1:p.Arg170del
XM_017013794.1:c.509_511del	XP_016869283.1:p.Arg170del
XM_017013795.1:c.509_511del	XP_016869284.1:p.Arg170del
XM_017013796.1:c.509_511del	XP_016869285.1:p.Arg170del
XM_017013797.1:c.248_250del	XP_016869286.1:p.Arg83del
XM_017013798.1:c.509_511del	XP_016869287.1:p.Arg170del
XM_017013799.1:c.509_511del	XP_016869288.1:p.Arg170del
XM_017013800.1:c.509_511del	XP_016869289.1:p.Arg170del
NM_003235.5:c.509_511del MANE Select	NP_003226.4:p.Arg170del