Canonical Allele Identifier: CA85865051

Gene: TIPARP

Linked Data

• dbSNP Id: rs905119429
• MyVariant Identifiers: chr3:g.156397543G>C (hg19) ; chr3:g.156679754G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.156679754G>C , CM000665.2:g.156679754G>C	GRCh38
NC_000003.11:g.156397543G>C , CM000665.1:g.156397543G>C	GRCh37
NC_000003.10:g.157880237G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295924.12:c.917+1140G>C MANE Select	ENSP00000295924.7:n.917+1140G>C
ENST00000295924.11:c.917+1140G>C	ENSP00000295924.7:n.917+1140G>C
ENST00000461166.5:c.917+1140G>C	ENSP00000420612.1:n.917+1140G>C
ENST00000473702.5:c.917+1140G>C	ENSP00000419982.1:n.917+1140G>C
ENST00000481853.5:c.917+1140G>C	ENSP00000418829.1:n.917+1140G>C
ENST00000486483.5:c.917+1140G>C	ENSP00000418757.1:n.917+1140G>C
ENST00000542783.5:c.917+1140G>C	ENSP00000438345.1:n.917+1140G>C
NM_001184717.1:c.917+1140G>C	NP_001171646.1:n.917+1140G>C
NM_001184718.1:c.917+1140G>C	NP_001171647.1:n.917+1140G>C
NM_015508.4:c.917+1140G>C	NP_056323.2:n.917+1140G>C
XM_011512668.1:c.917+1140G>C	XP_011510970.1:n.917+1140G>C
XM_011512669.1:c.918-720G>C	XP_011510971.1:n.918-720G>C
XR_001740978.1:n.1134G>C
NM_015508.5:c.917+1140G>C MANE Select	NP_056323.2:n.917+1140G>C
NM_001184718.2:c.917+1140G>C	NP_001171647.1:n.917+1140G>C