Canonical Allele Identifier: CA388287451

Gene: DIS3

Linked Data - Predicted Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.72772277T>C , CM000675.2:g.72772277T>C	GRCh38
NC_000013.10:g.73346415T>C , CM000675.1:g.73346415T>C	GRCh37
NC_000013.9:g.72244416T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377767.9:c.1387-2A>G MANE Select	ENSP00000366997.4:n.1387-2A>G
ENST00000377767.8:c.1387-2A>G	ENSP00000366997.4:n.1387-2A>G
ENST00000377780.8:c.1297-2A>G	ENSP00000367011.4:n.1297-2A>G
ENST00000490646.1:c.1387-2A>G	ENSP00000436350.1:n.1387-2A>G
ENST00000545453.5:c.901-2A>G	ENSP00000440058.1:n.901-2A>G
NM_001128226.2:c.1297-2A>G	NP_001121698.1:n.1297-2A>G
NM_014953.4:c.1387-2A>G	NP_055768.3:n.1387-2A>G
XM_005266294.1:c.901-2A>G	XP_005266351.1:n.901-2A>G
XM_006719778.1:c.1018-2A>G	XP_006719841.1:n.1018-2A>G
NM_001322348.1:c.1018-2A>G	NP_001309277.1:n.1018-2A>G
NM_001322349.1:c.901-2A>G	NP_001309278.1:n.901-2A>G
NM_014953.5:c.1387-2A>G MANE Select	NP_055768.3:n.1387-2A>G
NM_001128226.3:c.1297-2A>G	NP_001121698.1:n.1297-2A>G
NM_001322348.2:c.1018-2A>G	NP_001309277.1:n.1018-2A>G
NM_001322349.2:c.901-2A>G	NP_001309278.1:n.901-2A>G