Canonical Allele Identifier: CA1335214654

Gene: DIS3L2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232333840A= , CM000664.2:g.232333840A=	GRCh38
NC_000002.11:g.233198550A= , CM000664.1:g.233198550A=	GRCh37
NC_000002.10:g.232906794A=	NCBI36
NG_032572.1:g.377258A= , LRG_534:g.377258A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000325385.12:c.2011A= MANE Select	ENSP00000315569.7:p.Met671=
ENST00000273009.10:c.1582-9505A=	ENSP00000273009.6:n.1582-9505A=
ENST00000325385.11:c.2011A=	ENSP00000315569.7:p.Met671=
ENST00000390005.9:c.*78A=	ENSP00000374655.5:n.*78A=
ENST00000409307.5:c.2011A=	ENSP00000386799.1:p.Met671=
ENST00000424049.1:c.916A=	ENSP00000415419.1:p.Met306=
ENST00000429283.2:n.1577A=
ENST00000433430.5:c.3422A=	ENSP00000391175.1:n.3422A=
ENST00000445090.5:c.*1167A=	ENSP00000388999.1:n.*1167A=
NM_001257281.1:c.1582-9505A=	NP_001244210.1:n.1582-9505A=
NM_152383.4:c.2011A= , LRG_534t1:c.2011A=	NP_689596.4:p.Met671=
NR_046476.1:n.2214A=
NR_046477.1:n.2193A=
NM_001257281.2:c.1582-9505A=	NP_001244210.1:n.1582-9505A=
NM_152383.5:c.2011A= MANE Select	NP_689596.4:p.Met671=
NR_046476.2:n.2084A=
NR_046477.2:n.2063A=