Canonical Allele Identifier: CA351152068

Gene: DIS3L2

Linked Data

• MyVariant Identifiers: chr2:g.232880349T>A (hg19) ; chr2:g.232015639T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232015639T>A , CM000664.2:g.232015639T>A	GRCh38
NC_000002.11:g.232880349T>A , CM000664.1:g.232880349T>A	GRCh37
NC_000002.10:g.232588593T>A	NCBI36
NG_032572.1:g.59057T>A , LRG_534:g.59057T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325385.12:c.178T>A MANE Select	ENSP00000315569.7:p.Ser60Thr
ENST00000273009.10:c.178T>A	ENSP00000273009.6:p.Ser60Thr
ENST00000325385.11:c.178T>A	ENSP00000315569.7:p.Ser60Thr
ENST00000390005.9:c.178T>A	ENSP00000374655.5:p.Ser60Thr
ENST00000409307.5:c.178T>A	ENSP00000386799.1:p.Ser60Thr
ENST00000409401.7:c.178T>A	ENSP00000386594.3:p.Ser60Thr
ENST00000433430.5:c.178T>A	ENSP00000391175.1:p.Ser60Thr
ENST00000441279.5:c.178T>A	ENSP00000390467.1:p.Ser60Thr
ENST00000445090.5:c.178T>A	ENSP00000388999.1:p.Ser60Thr
ENST00000464554.5:n.39T>A
NM_001257281.1:c.178T>A	NP_001244210.1:p.Ser60Thr
NM_001257282.1:c.178T>A	NP_001244211.1:p.Ser60Thr
NM_152383.4:c.178T>A , LRG_534t1:c.178T>A	NP_689596.4:p.Ser60Thr
NR_046476.1:n.454T>A
NR_046477.1:n.454T>A
NM_001257281.2:c.178T>A	NP_001244210.1:p.Ser60Thr
NM_152383.5:c.178T>A MANE Select	NP_689596.4:p.Ser60Thr
NR_046476.2:n.324T>A
NR_046477.2:n.324T>A
NM_001257282.2:c.178T>A	NP_001244211.1:p.Ser60Thr