Canonical Allele Identifier: CA4094822

Gene: RNASET2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.166929699C>T , CM000668.2:g.166929699C>T	GRCh38
NC_000006.11:g.167343187C>T , CM000668.1:g.167343187C>T	GRCh37
NC_000006.10:g.167263177C>T	NCBI36
NG_016280.1:g.31891G>A
NG_016280.2:g.31891G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003730.6:c.660G>A MANE Select	NP_003721.2:p.Pro220=
ENST00000508775.6:c.660G>A MANE Select	ENSP00000426455.2:p.Pro220=
NM_003730.4:c.660G>A	NP_003721.2:p.Pro220=
NM_003730.5:c.660G>A	NP_003721.2:p.Pro220=
ENST00000028008.9:c.*448G>A	ENSP00000028008.5:n.*448G>A
ENST00000366855.10:c.546G>A	ENSP00000424947.1:p.Pro182=
ENST00000421787.5:c.*1014G>A	ENSP00000390833.1:n.*1014G>A
ENST00000467705.6:n.458G>A
ENST00000476238.6:c.660G>A	ENSP00000422846.1:p.Pro220=
ENST00000478180.6:c.660G>A	ENSP00000426059.1:p.Pro220=
ENST00000507747.1:c.434+4392G>A
ENST00000508775.5:c.660G>A	ENSP00000426455.1:p.Pro220=
ENST00000510083.1:n.2099G>A
ENST00000611959.2:c.*448G>A	ENSP00000480244.2:n.*448G>A
ENST00000620173.4:c.810G>A	ENSP00000482755.1:p.Pro270=
ENST00000620173.5:c.546G>A	ENSP00000482755.2:p.Pro182=
ENST00000682498.1:n.2778G>A
ENST00000682774.1:c.*501G>A	ENSP00000507399.1:n.*501G>A
ENST00000683770.1:c.414G>A	ENSP00000507710.1:p.Pro138=
ENST00000683968.1:n.3152G>A
ENST00000684236.1:c.384G>A	ENSP00000508128.1:p.Pro128=
XM_017011397.1:c.546G>A	XP_016866886.1:p.Pro182=
XM_017011398.1:c.384G>A	XP_016866887.1:p.Pro128=
XM_017011399.1:c.*125G>A	XP_016866888.1:n.*125G>A
XM_024446575.1:c.384G>A	XP_024302343.1:p.Pro128=
XM_024446576.1:c.384G>A	XP_024302344.1:p.Pro128=