Canonical Allele Identifier: CA4095110

Gene: RNASET2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.166946736G>A , CM000668.2:g.166946736G>A	GRCh38
NC_000006.11:g.167360224G>A , CM000668.1:g.167360224G>A	GRCh37
NC_000006.10:g.167280214G>A	NCBI36
NG_016280.1:g.14854C>T
NG_016280.2:g.14854C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003730.6:c.207C>T MANE Select	NP_003721.2:p.Pro69=
ENST00000508775.6:c.207C>T MANE Select	ENSP00000426455.2:p.Pro69=
NM_003730.4:c.207C>T	NP_003721.2:p.Pro69=
NM_003730.5:c.207C>T	NP_003721.2:p.Pro69=
ENST00000028008.9:c.211C>T	ENSP00000028008.5:p.Arg71Ter
ENST00000358165.7:n.244-3647C>T
ENST00000366855.10:c.93C>T	ENSP00000424947.1:p.Pro31=
ENST00000421787.5:c.207C>T	ENSP00000390833.1:p.Pro69=
ENST00000476238.6:c.207C>T	ENSP00000422846.1:p.Pro69=
ENST00000478180.6:c.207C>T	ENSP00000426059.1:p.Pro69=
ENST00000496851.6:n.107C>T
ENST00000499370.6:n.1153C>T
ENST00000507747.1:c.149C>T
ENST00000508775.5:c.207C>T	ENSP00000426455.1:p.Pro69=
ENST00000611959.1:c.207C>T	ENSP00000480244.1:p.Pro69=
ENST00000611959.2:c.151C>T	ENSP00000480244.2:p.Arg51Ter
ENST00000620173.4:c.207C>T	ENSP00000482755.1:p.Pro69=
ENST00000620173.5:c.148-3647C>T	ENSP00000482755.2:n.148-3647C>T
ENST00000682498.1:n.2325C>T
ENST00000682774.1:c.207C>T	ENSP00000507399.1:p.Pro69=
ENST00000683158.1:n.368C>T
ENST00000683770.1:c.87-7728C>T	ENSP00000507710.1:n.87-7728C>T
ENST00000683968.1:n.2699C>T
ENST00000684236.1:c.-70C>T	ENSP00000508128.1:n.-70C>T
XM_017011397.1:c.93C>T	XP_016866886.1:p.Pro31=
XM_017011398.1:c.-70C>T	XP_016866887.1:n.-70C>T
XM_017011399.1:c.207C>T	XP_016866888.1:p.Pro69=
XM_024446575.1:c.-70C>T	XP_024302343.1:n.-70C>T
XM_024446576.1:c.-70C>T	XP_024302344.1:n.-70C>T