Canonical Allele Identifier: CA11140681

Gene: DIS3L2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232290400T>C , CM000664.2:g.232290400T>C	GRCh38
NC_000002.11:g.233155110T>C , CM000664.1:g.233155110T>C	GRCh37
NC_000002.10:g.232863354T>C	NCBI36
NG_032572.1:g.333818T>C , LRG_534:g.333818T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325385.12:c.1660-9640T>C MANE Select	ENSP00000315569.7:n.1660-9640T>C
ENST00000273009.10:c.1581+27038T>C	ENSP00000273009.6:n.1581+27038T>C
ENST00000325385.11:c.1660-9640T>C	ENSP00000315569.7:n.1660-9640T>C
ENST00000390005.9:c.1660-9640T>C	ENSP00000374655.5:n.1660-9640T>C
ENST00000409307.5:c.1660-9640T>C	ENSP00000386799.1:n.1660-9640T>C
ENST00000424049.1:c.565-9640T>C	ENSP00000415419.1:n.565-9640T>C
ENST00000433430.5:c.2814-9640T>C	ENSP00000391175.1:n.2814-9640T>C
ENST00000445090.5:c.*886-9640T>C	ENSP00000388999.1:n.*886-9640T>C
ENST00000498319.2:n.242-9640T>C
NM_001257281.1:c.1581+27038T>C	NP_001244210.1:n.1581+27038T>C
NM_152383.4:c.1660-9640T>C , LRG_534t1:c.1660-9640T>C	NP_689596.4:n.1660-9640T>C
NR_046476.1:n.1936-9640T>C
NR_046477.1:n.1912-9640T>C
NM_001257281.2:c.1581+27038T>C	NP_001244210.1:n.1581+27038T>C
NM_152383.5:c.1660-9640T>C MANE Select	NP_689596.4:n.1660-9640T>C
NR_046476.2:n.1806-9640T>C
NR_046477.2:n.1782-9640T>C