Canonical Allele Identifier: CA1413459938
Gene: TIPARP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.156680170_156680174delinsAAAGT , CM000665.2:g.156680170_156680174delinsAAAGT GRCh38
NC_000003.11:g.156397959_156397963delinsAAAGT , CM000665.1:g.156397959_156397963delinsAAAGT GRCh37
NC_000003.10:g.157880653_157880657delinsAAAGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295924.12:c.917+1556_917+1560delinsAAAGT MANE Select ENSP00000295924.7:n.917+1556_917+1560delinsAAAGT
ENST00000295924.11:c.917+1556_917+1560delinsAAAGT ENSP00000295924.7:n.917+1556_917+1560delinsAAAGT
ENST00000461166.5:c.917+1556_917+1560delinsAAAGT ENSP00000420612.1:n.917+1556_917+1560delinsAAAGT
ENST00000473702.5:c.917+1556_917+1560delinsAAAGT ENSP00000419982.1:n.917+1556_917+1560delinsAAAGT
ENST00000481853.5:c.917+1556_917+1560delinsAAAGT ENSP00000418829.1:n.917+1556_917+1560delinsAAAGT
ENST00000486483.5:c.917+1556_917+1560delinsAAAGT ENSP00000418757.1:n.917+1556_917+1560delinsAAAGT
ENST00000542783.5:c.917+1556_917+1560delinsAAAGT ENSP00000438345.1:n.917+1556_917+1560delinsAAAGT
NM_001184717.1:c.917+1556_917+1560delinsAAAGT NP_001171646.1:n.917+1556_917+1560delinsAAAGT
NM_001184718.1:c.917+1556_917+1560delinsAAAGT NP_001171647.1:n.917+1556_917+1560delinsAAAGT
NM_015508.4:c.917+1556_917+1560delinsAAAGT NP_056323.2:n.917+1556_917+1560delinsAAAGT
XM_011512668.1:c.917+1556_917+1560delinsAAAGT XP_011510970.1:n.917+1556_917+1560delinsAAAGT
XM_011512669.1:c.918-304_918-300delinsAAAGT XP_011510971.1:n.918-304_918-300delinsAAAGT
XR_001740978.1:n.1550_1554delinsAAAGT
NM_015508.5:c.917+1556_917+1560delinsAAAGT MANE Select NP_056323.2:n.917+1556_917+1560delinsAAAGT
NM_001184718.2:c.917+1556_917+1560delinsAAAGT NP_001171647.1:n.917+1556_917+1560delinsAAAGT