Canonical Allele Identifier: CA1055311862
Gene: TIPARP HGNC NCBI

Linked Data

dbSNP Id: rs1722259866

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.156680214_156680217dup , CM000665.2:g.156680214_156680217dup GRCh38
NC_000003.11:g.156398003_156398006dup , CM000665.1:g.156398003_156398006dup GRCh37
NC_000003.10:g.157880697_157880700dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295924.12:c.917+1600_917+1603dup MANE Select ENSP00000295924.7:n.917+1600_917+1603dup
ENST00000295924.11:c.917+1600_917+1603dup ENSP00000295924.7:n.917+1600_917+1603dup
ENST00000461166.5:c.917+1600_917+1603dup ENSP00000420612.1:n.917+1600_917+1603dup
ENST00000473702.5:c.917+1600_917+1603dup ENSP00000419982.1:n.917+1600_917+1603dup
ENST00000481853.5:c.917+1600_917+1603dup ENSP00000418829.1:n.917+1600_917+1603dup
ENST00000486483.5:c.917+1600_917+1603dup ENSP00000418757.1:n.917+1600_917+1603dup
ENST00000542783.5:c.917+1600_917+1603dup ENSP00000438345.1:n.917+1600_917+1603dup
NM_001184717.1:c.917+1600_917+1603dup NP_001171646.1:n.917+1600_917+1603dup
NM_001184718.1:c.917+1600_917+1603dup NP_001171647.1:n.917+1600_917+1603dup
NM_015508.4:c.917+1600_917+1603dup NP_056323.2:n.917+1600_917+1603dup
XM_011512668.1:c.917+1600_917+1603dup XP_011510970.1:n.917+1600_917+1603dup
XM_011512669.1:c.918-260_918-257dup XP_011510971.1:n.918-260_918-257dup
XR_001740978.1:n.1594_1597dup
NM_015508.5:c.917+1600_917+1603dup MANE Select NP_056323.2:n.917+1600_917+1603dup
NM_001184718.2:c.917+1600_917+1603dup NP_001171647.1:n.917+1600_917+1603dup