Canonical Allele Identifier: CA1413459751

Gene: TIPARP

Linked Data

• dbSNP Id: rs2665390

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.156679960C>G , CM000665.2:g.156679960C>G	GRCh38
NC_000003.11:g.156397749C>G , CM000665.1:g.156397749C>G	GRCh37
NC_000003.10:g.157880443C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000295924.12:c.917+1346C>G MANE Select	ENSP00000295924.7:n.917+1346C>G
ENST00000295924.11:c.917+1346C>G	ENSP00000295924.7:n.917+1346C>G
ENST00000461166.5:c.917+1346C>G	ENSP00000420612.1:n.917+1346C>G
ENST00000473702.5:c.917+1346C>G	ENSP00000419982.1:n.917+1346C>G
ENST00000481853.5:c.917+1346C>G	ENSP00000418829.1:n.917+1346C>G
ENST00000486483.5:c.917+1346C>G	ENSP00000418757.1:n.917+1346C>G
ENST00000542783.5:c.917+1346C>G	ENSP00000438345.1:n.917+1346C>G
NM_001184717.1:c.917+1346C>G	NP_001171646.1:n.917+1346C>G
NM_001184718.1:c.917+1346C>G	NP_001171647.1:n.917+1346C>G
NM_015508.4:c.917+1346C>G	NP_056323.2:n.917+1346C>G
XM_011512668.1:c.917+1346C>G	XP_011510970.1:n.917+1346C>G
XM_011512669.1:c.918-514C>G	XP_011510971.1:n.918-514C>G
XR_001740978.1:n.1340C>G
NM_015508.5:c.917+1346C>G MANE Select	NP_056323.2:n.917+1346C>G
NM_001184718.2:c.917+1346C>G	NP_001171647.1:n.917+1346C>G