Canonical Allele Identifier: CA1055311794

Gene: TIPARP

Linked Data

• dbSNP Id: rs1722253107
• gnomAD v3: 3-156680003-T-TTTCAGTTATATAGTACATATTTCAGTTATATAGTACA
• gnomAD v4: 3-156680003-T-TTTCAGTTATATAGTACATATTTCAGTTATATAGTACA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.156680004_156680005insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT , CM000665.2:g.156680004_156680005insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT	GRCh38
NC_000003.11:g.156397793_156397794insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT , CM000665.1:g.156397793_156397794insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT	GRCh37
NC_000003.10:g.157880487_157880488insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000295924.12:c.917+1390_917+1391insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT MANE Select	ENSP00000295924.7:n.917+1390_917+1391insTCAGTTATATAGTACATATTT...
ENST00000295924.11:c.917+1390_917+1391insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT	ENSP00000295924.7:n.917+1390_917+1391insTCAGTTATATAGTACATATTT...
ENST00000461166.5:c.917+1390_917+1391insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT	ENSP00000420612.1:n.917+1390_917+1391insTCAGTTATATAGTACATATTT...
ENST00000473702.5:c.917+1390_917+1391insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT	ENSP00000419982.1:n.917+1390_917+1391insTCAGTTATATAGTACATATTT...
ENST00000481853.5:c.917+1390_917+1391insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT	ENSP00000418829.1:n.917+1390_917+1391insTCAGTTATATAGTACATATTT...
ENST00000486483.5:c.917+1390_917+1391insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT	ENSP00000418757.1:n.917+1390_917+1391insTCAGTTATATAGTACATATTT...
ENST00000542783.5:c.917+1390_917+1391insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT	ENSP00000438345.1:n.917+1390_917+1391insTCAGTTATATAGTACATATTT...
NM_001184717.1:c.917+1390_917+1391insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT	NP_001171646.1:n.917+1390_917+1391insTCAGTTATATAGTACATATTTCAG...
NM_001184718.1:c.917+1390_917+1391insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT	NP_001171647.1:n.917+1390_917+1391insTCAGTTATATAGTACATATTTCAG...
NM_015508.4:c.917+1390_917+1391insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT	NP_056323.2:n.917+1390_917+1391insTCAGTTATATAGTACATATTTCAGTTA...
XM_011512668.1:c.917+1390_917+1391insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT	XP_011510970.1:n.917+1390_917+1391insTCAGTTATATAGTACATATTTCAG...
XM_011512669.1:c.918-470_918-469insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT	XP_011510971.1:n.918-470_918-469insTCAGTTATATAGTACATATTTCAGTT...
XR_001740978.1:n.1384_1385insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT
NM_015508.5:c.917+1390_917+1391insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT MANE Select	NP_056323.2:n.917+1390_917+1391insTCAGTTATATAGTACATATTTCAGTTA...
NM_001184718.2:c.917+1390_917+1391insTCAGTTATATAGTACATATTTCAGTTATATAGTACAT	NP_001171647.1:n.917+1390_917+1391insTCAGTTATATAGTACATATTTCAG...