Canonical Allele Identifier: CA431908840

Gene: DIS3L2

Linked Data

• MyVariant Identifiers: chr2:g.232880297A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232015587A>G , CM000664.2:g.232015587A>G	GRCh38
NC_000002.11:g.232880297A>G , CM000664.1:g.232880297A>G	GRCh37
NC_000002.10:g.232588541A>G	NCBI36
NG_032572.1:g.59005A>G , LRG_534:g.59005A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325385.12:c.126A>G MANE Select	ENSP00000315569.7:p.Thr42=
ENST00000273009.10:c.126A>G	ENSP00000273009.6:p.Thr42=
ENST00000325385.11:c.126A>G	ENSP00000315569.7:p.Thr42=
ENST00000390005.9:c.126A>G	ENSP00000374655.5:p.Thr42=
ENST00000409307.5:c.126A>G	ENSP00000386799.1:p.Thr42=
ENST00000409401.7:c.126A>G	ENSP00000386594.3:p.Thr42=
ENST00000433430.5:c.126A>G	ENSP00000391175.1:p.Thr42=
ENST00000441279.5:c.126A>G	ENSP00000390467.1:p.Thr42=
ENST00000445090.5:c.126A>G	ENSP00000388999.1:p.Thr42=
NM_001257281.1:c.126A>G	NP_001244210.1:p.Thr42=
NM_001257282.1:c.126A>G	NP_001244211.1:p.Thr42=
NM_152383.4:c.126A>G , LRG_534t1:c.126A>G	NP_689596.4:p.Thr42=
NR_046476.1:n.402A>G
NR_046477.1:n.402A>G
NM_001257281.2:c.126A>G	NP_001244210.1:p.Thr42=
NM_152383.5:c.126A>G MANE Select	NP_689596.4:p.Thr42=
NR_046476.2:n.272A>G
NR_046477.2:n.272A>G
NM_001257282.2:c.126A>G	NP_001244211.1:p.Thr42=