Canonical Allele Identifier: CA4095016

Gene: RNASET2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.166938961G>A , CM000668.2:g.166938961G>A	GRCh38
NC_000006.11:g.167352449G>A , CM000668.1:g.167352449G>A	GRCh37
NC_000006.10:g.167272439G>A	NCBI36
NG_016280.1:g.22629C>T
NG_016280.2:g.22629C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003730.6:c.380C>T MANE Select	NP_003721.2:p.Ala127Val
ENST00000508775.6:c.380C>T MANE Select	ENSP00000426455.2:p.Ala127Val
NM_003730.4:c.380C>T	NP_003721.2:p.Ala127Val
NM_003730.5:c.380C>T	NP_003721.2:p.Ala127Val
ENST00000028008.9:c.*168C>T	ENSP00000028008.5:n.*168C>T
ENST00000358165.7:n.362C>T
ENST00000366855.10:c.266C>T	ENSP00000424947.1:p.Ala89Val
ENST00000421787.5:c.*734C>T	ENSP00000390833.1:n.*734C>T
ENST00000467705.6:n.178C>T
ENST00000476238.6:c.380C>T	ENSP00000422846.1:p.Ala127Val
ENST00000478180.6:c.380C>T	ENSP00000426059.1:p.Ala127Val
ENST00000496851.6:n.280C>T
ENST00000499370.6:n.1326C>T
ENST00000507747.1:c.322C>T
ENST00000508775.5:c.380C>T	ENSP00000426455.1:p.Ala127Val
ENST00000509073.1:n.269C>T
ENST00000611959.1:c.334C>T	ENSP00000480244.1:p.Arg112Cys
ENST00000611959.2:c.*168C>T	ENSP00000480244.2:n.*168C>T
ENST00000620173.4:c.530C>T	ENSP00000482755.1:p.Ala177Val
ENST00000620173.5:c.266C>T	ENSP00000482755.2:p.Ala89Val
ENST00000682498.1:n.2498C>T
ENST00000682774.1:c.*221C>T	ENSP00000507399.1:n.*221C>T
ENST00000683770.1:c.134C>T	ENSP00000507710.1:p.Ala45Val
ENST00000683968.1:n.2872C>T
ENST00000684086.1:n.1427C>T
ENST00000684236.1:c.104C>T	ENSP00000508128.1:p.Ala35Val
XM_017011397.1:c.266C>T	XP_016866886.1:p.Ala89Val
XM_017011398.1:c.104C>T	XP_016866887.1:p.Ala35Val
XM_017011399.1:c.380C>T	XP_016866888.1:p.Ala127Val
XM_024446575.1:c.104C>T	XP_024302343.1:p.Ala35Val
XM_024446576.1:c.104C>T	XP_024302344.1:p.Ala35Val