Canonical Allele Identifier: CA1335214653

Gene: DIS3L2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232333839G= , CM000664.2:g.232333839G=	GRCh38
NC_000002.11:g.233198549G= , CM000664.1:g.233198549G=	GRCh37
NC_000002.10:g.232906793G=	NCBI36
NG_032572.1:g.377257G= , LRG_534:g.377257G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000325385.12:c.2011-1G= MANE Select	ENSP00000315569.7:n.2011-1G=
ENST00000273009.10:c.1582-9506G=	ENSP00000273009.6:n.1582-9506G=
ENST00000325385.11:c.2011-1G=	ENSP00000315569.7:n.2011-1G=
ENST00000390005.9:c.*78-1G=	ENSP00000374655.5:n.*78-1G=
ENST00000409307.5:c.2011-1G=	ENSP00000386799.1:n.2011-1G=
ENST00000424049.1:c.916-1G=	ENSP00000415419.1:n.916-1G=
ENST00000429283.2:n.1577-1G=
ENST00000433430.5:c.3422-1G=	ENSP00000391175.1:n.3422-1G=
ENST00000445090.5:c.*1167-1G=	ENSP00000388999.1:n.*1167-1G=
NM_001257281.1:c.1582-9506G=	NP_001244210.1:n.1582-9506G=
NM_152383.4:c.2011-1G= , LRG_534t1:c.2011-1G=	NP_689596.4:n.2011-1G=
NR_046476.1:n.2214-1G=
NR_046477.1:n.2193-1G=
NM_001257281.2:c.1582-9506G=	NP_001244210.1:n.1582-9506G=
NM_152383.5:c.2011-1G= MANE Select	NP_689596.4:n.2011-1G=
NR_046476.2:n.2084-1G=
NR_046477.2:n.2063-1G=