Canonical Allele Identifier: CA1055311816

Gene: TIPARP

Linked Data

• dbSNP Id: rs1722256113
• gnomAD v3: 3-156680075-T-TA
• gnomAD v4: 3-156680075-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.156680075_156680076insA , CM000665.2:g.156680075_156680076insA	GRCh38
NC_000003.11:g.156397864_156397865insA , CM000665.1:g.156397864_156397865insA	GRCh37
NC_000003.10:g.157880558_157880559insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295924.12:c.917+1461_917+1462insA MANE Select	ENSP00000295924.7:n.917+1461_917+1462insA
ENST00000295924.11:c.917+1461_917+1462insA	ENSP00000295924.7:n.917+1461_917+1462insA
ENST00000461166.5:c.917+1461_917+1462insA	ENSP00000420612.1:n.917+1461_917+1462insA
ENST00000473702.5:c.917+1461_917+1462insA	ENSP00000419982.1:n.917+1461_917+1462insA
ENST00000481853.5:c.917+1461_917+1462insA	ENSP00000418829.1:n.917+1461_917+1462insA
ENST00000486483.5:c.917+1461_917+1462insA	ENSP00000418757.1:n.917+1461_917+1462insA
ENST00000542783.5:c.917+1461_917+1462insA	ENSP00000438345.1:n.917+1461_917+1462insA
NM_001184717.1:c.917+1461_917+1462insA	NP_001171646.1:n.917+1461_917+1462insA
NM_001184718.1:c.917+1461_917+1462insA	NP_001171647.1:n.917+1461_917+1462insA
NM_015508.4:c.917+1461_917+1462insA	NP_056323.2:n.917+1461_917+1462insA
XM_011512668.1:c.917+1461_917+1462insA	XP_011510970.1:n.917+1461_917+1462insA
XM_011512669.1:c.918-399_918-398insA	XP_011510971.1:n.918-399_918-398insA
XR_001740978.1:n.1455_1456insA
NM_015508.5:c.917+1461_917+1462insA MANE Select	NP_056323.2:n.917+1461_917+1462insA
NM_001184718.2:c.917+1461_917+1462insA	NP_001171647.1:n.917+1461_917+1462insA