Canonical Allele Identifier: CA388289175

Gene: DIS3

Linked Data - Expert Curation

Linked Data - Predicted Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.72775209A>G , CM000675.2:g.72775209A>G	GRCh38
NC_000013.10:g.73349347A>G , CM000675.1:g.73349347A>G	GRCh37
NC_000013.9:g.72247348A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377767.9:c.987+2T>C MANE Select	ENSP00000366997.4:n.987+2T>C
ENST00000377767.8:c.987+2T>C	ENSP00000366997.4:n.987+2T>C
ENST00000377780.8:c.897+2T>C	ENSP00000367011.4:n.897+2T>C
ENST00000490646.1:c.987+2T>C	ENSP00000436350.1:n.987+2T>C
ENST00000545453.5:c.501+2T>C	ENSP00000440058.1:n.501+2T>C
NM_001128226.2:c.897+2T>C	NP_001121698.1:n.897+2T>C
NM_014953.4:c.987+2T>C	NP_055768.3:n.987+2T>C
XM_005266294.1:c.501+2T>C	XP_005266351.1:n.501+2T>C
XM_006719778.1:c.618+2T>C	XP_006719841.1:n.618+2T>C
NM_001322348.1:c.618+2T>C	NP_001309277.1:n.618+2T>C
NM_001322349.1:c.501+2T>C	NP_001309278.1:n.501+2T>C
NM_014953.5:c.987+2T>C MANE Select	NP_055768.3:n.987+2T>C
NM_001128226.3:c.897+2T>C	NP_001121698.1:n.897+2T>C
NM_001322348.2:c.618+2T>C	NP_001309277.1:n.618+2T>C
NM_001322349.2:c.501+2T>C	NP_001309278.1:n.501+2T>C