Canonical Allele Identifier: CA1335162624

Gene: DIS3L2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232212354A= , CM000664.2:g.232212354A=	GRCh38
NC_000002.11:g.233077064A= , CM000664.1:g.233077064A=	GRCh37
NC_000002.10:g.232785308A=	NCBI36
NG_032572.1:g.255772A= , LRG_534:g.255772A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325385.12:c.1204+1949A= MANE Select	ENSP00000315569.7:n.1204+1949A=
ENST00000273009.10:c.1204+1949A=	ENSP00000273009.6:n.1204+1949A=
ENST00000325385.11:c.1204+1949A=	ENSP00000315569.7:n.1204+1949A=
ENST00000390005.9:c.1204+1949A=	ENSP00000374655.5:n.1204+1949A=
ENST00000409307.5:c.1204+1949A=	ENSP00000386799.1:n.1204+1949A=
ENST00000424049.1:c.109+1949A=	ENSP00000415419.1:n.109+1949A=
ENST00000433430.5:c.1513+1949A=	ENSP00000391175.1:n.1513+1949A=
ENST00000445090.5:c.*430+1949A=	ENSP00000388999.1:n.*430+1949A=
NM_001257281.1:c.1204+1949A=	NP_001244210.1:n.1204+1949A=
NM_152383.4:c.1204+1949A= , LRG_534t1:c.1204+1949A=	NP_689596.4:n.1204+1949A=
NR_046476.1:n.1480+1949A=
NR_046477.1:n.1456+1949A=
NM_001257281.2:c.1204+1949A=	NP_001244210.1:n.1204+1949A=
NM_152383.5:c.1204+1949A= MANE Select	NP_689596.4:n.1204+1949A=
NR_046476.2:n.1350+1949A=
NR_046477.2:n.1326+1949A=