Canonical Allele Identifier: CA366407846

Gene: RNASET2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.166946710G>T , CM000668.2:g.166946710G>T	GRCh38
NC_000006.11:g.167360198G>T , CM000668.1:g.167360198G>T	GRCh37
NC_000006.10:g.167280188G>T	NCBI36
NG_016280.1:g.14880C>A
NG_016280.2:g.14880C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003730.6:c.233C>A MANE Select	NP_003721.2:p.Ser78Ter
ENST00000508775.6:c.233C>A MANE Select	ENSP00000426455.2:p.Ser78Ter
NM_003730.4:c.233C>A	NP_003721.2:p.Ser78Ter
NM_003730.5:c.233C>A	NP_003721.2:p.Ser78Ter
ENST00000028008.9:c.*21C>A	ENSP00000028008.5:n.*21C>A
ENST00000358165.7:n.244-3621C>A
ENST00000366855.10:c.119C>A	ENSP00000424947.1:p.Ser40Ter
ENST00000421787.5:c.233C>A	ENSP00000390833.1:p.Ser78Ter
ENST00000476238.6:c.233C>A	ENSP00000422846.1:p.Ser78Ter
ENST00000478180.6:c.233C>A	ENSP00000426059.1:p.Ser78Ter
ENST00000496851.6:n.133C>A
ENST00000499370.6:n.1179C>A
ENST00000507747.1:c.175C>A
ENST00000508775.5:c.233C>A	ENSP00000426455.1:p.Ser78Ter
ENST00000611959.1:c.233C>A	ENSP00000480244.1:p.Ser78Ter
ENST00000611959.2:c.*21C>A	ENSP00000480244.2:n.*21C>A
ENST00000620173.4:c.233C>A	ENSP00000482755.1:p.Ser78Ter
ENST00000620173.5:c.148-3621C>A	ENSP00000482755.2:n.148-3621C>A
ENST00000682498.1:n.2351C>A
ENST00000682774.1:c.233C>A	ENSP00000507399.1:p.Ser78Ter
ENST00000683158.1:n.394C>A
ENST00000683770.1:c.87-7702C>A	ENSP00000507710.1:n.87-7702C>A
ENST00000683968.1:n.2725C>A
ENST00000684236.1:c.-44C>A	ENSP00000508128.1:n.-44C>A
XM_017011397.1:c.119C>A	XP_016866886.1:p.Ser40Ter
XM_017011398.1:c.-44C>A	XP_016866887.1:n.-44C>A
XM_017011399.1:c.233C>A	XP_016866888.1:p.Ser78Ter
XM_024446575.1:c.-44C>A	XP_024302343.1:n.-44C>A
XM_024446576.1:c.-44C>A	XP_024302344.1:n.-44C>A