Canonical Allele Identifier: CA431779082

Gene: DIS3L2

Linked Data

• MyVariant Identifiers: chr2:g.233198558G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232333848G>C , CM000664.2:g.232333848G>C	GRCh38
NC_000002.11:g.233198558G>C , CM000664.1:g.233198558G>C	GRCh37
NC_000002.10:g.232906802G>C	NCBI36
NG_032572.1:g.377266G>C , LRG_534:g.377266G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000325385.12:c.2019G>C MANE Select	ENSP00000315569.7:p.Leu673=
ENST00000273009.10:c.1582-9497G>C	ENSP00000273009.6:n.1582-9497G>C
ENST00000325385.11:c.2019G>C	ENSP00000315569.7:p.Leu673=
ENST00000390005.9:c.*86G>C	ENSP00000374655.5:n.*86G>C
ENST00000409307.5:c.2019G>C	ENSP00000386799.1:p.Leu673=
ENST00000424049.1:c.924G>C	ENSP00000415419.1:p.Leu308=
ENST00000429283.2:n.1585G>C
ENST00000433430.5:c.3430G>C	ENSP00000391175.1:n.3430G>C
ENST00000445090.5:c.*1175G>C	ENSP00000388999.1:n.*1175G>C
NM_001257281.1:c.1582-9497G>C	NP_001244210.1:n.1582-9497G>C
NM_152383.4:c.2019G>C , LRG_534t1:c.2019G>C	NP_689596.4:p.Leu673=
NR_046476.1:n.2222G>C
NR_046477.1:n.2201G>C
NM_001257281.2:c.1582-9497G>C	NP_001244210.1:n.1582-9497G>C
NM_152383.5:c.2019G>C MANE Select	NP_689596.4:p.Leu673=
NR_046476.2:n.2092G>C
NR_046477.2:n.2071G>C