Canonical Allele Identifier: CA4095004

Gene: RNASET2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.166938915G>A , CM000668.2:g.166938915G>A	GRCh38
NC_000006.11:g.167352403G>A , CM000668.1:g.167352403G>A	GRCh37
NC_000006.10:g.167272393G>A	NCBI36
NG_016280.1:g.22675C>T
NG_016280.2:g.22675C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003730.6:c.426C>T MANE Select	NP_003721.2:p.Tyr142=
ENST00000508775.6:c.426C>T MANE Select	ENSP00000426455.2:p.Tyr142=
NM_003730.4:c.426C>T	NP_003721.2:p.Tyr142=
NM_003730.5:c.426C>T	NP_003721.2:p.Tyr142=
ENST00000028008.9:c.*214C>T	ENSP00000028008.5:n.*214C>T
ENST00000358165.7:n.408C>T
ENST00000366855.10:c.312C>T	ENSP00000424947.1:p.Tyr104=
ENST00000421787.5:c.*780C>T	ENSP00000390833.1:n.*780C>T
ENST00000467705.6:n.224C>T
ENST00000476238.6:c.426C>T	ENSP00000422846.1:p.Tyr142=
ENST00000478180.6:c.426C>T	ENSP00000426059.1:p.Tyr142=
ENST00000496851.6:n.326C>T
ENST00000499370.6:n.1372C>T
ENST00000507747.1:c.368C>T
ENST00000508775.5:c.426C>T	ENSP00000426455.1:p.Tyr142=
ENST00000509073.1:n.315C>T
ENST00000611959.1:c.380C>T	ENSP00000480244.1:p.Thr127Ile
ENST00000611959.2:c.*214C>T	ENSP00000480244.2:n.*214C>T
ENST00000620173.4:c.576C>T	ENSP00000482755.1:p.Tyr192=
ENST00000620173.5:c.312C>T	ENSP00000482755.2:p.Tyr104=
ENST00000682498.1:n.2544C>T
ENST00000682774.1:c.*267C>T	ENSP00000507399.1:n.*267C>T
ENST00000683770.1:c.180C>T	ENSP00000507710.1:p.Tyr60=
ENST00000683968.1:n.2918C>T
ENST00000684086.1:n.1473C>T
ENST00000684236.1:c.150C>T	ENSP00000508128.1:p.Tyr50=
XM_017011397.1:c.312C>T	XP_016866886.1:p.Tyr104=
XM_017011398.1:c.150C>T	XP_016866887.1:p.Tyr50=
XM_017011399.1:c.426C>T	XP_016866888.1:p.Tyr142=
XM_024446575.1:c.150C>T	XP_024302343.1:p.Tyr50=
XM_024446576.1:c.150C>T	XP_024302344.1:p.Tyr50=