Canonical Allele Identifier: CA4094843

Gene: RNASET2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.166929795A>G , CM000668.2:g.166929795A>G	GRCh38
NC_000006.11:g.167343283A>G , CM000668.1:g.167343283A>G	GRCh37
NC_000006.10:g.167263273A>G	NCBI36
NG_016280.1:g.31795T>C
NG_016280.2:g.31795T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003730.6:c.568-4T>C MANE Select	NP_003721.2:n.568-4T>C
ENST00000508775.6:c.568-4T>C MANE Select	ENSP00000426455.2:n.568-4T>C
NM_003730.4:c.568-4T>C	NP_003721.2:n.568-4T>C
NM_003730.5:c.568-4T>C	NP_003721.2:n.568-4T>C
ENST00000028008.9:c.*356-4T>C	ENSP00000028008.5:n.*356-4T>C
ENST00000366855.10:c.454-4T>C	ENSP00000424947.1:n.454-4T>C
ENST00000421787.5:c.*922-4T>C	ENSP00000390833.1:n.*922-4T>C
ENST00000467705.6:n.366-4T>C
ENST00000476238.6:c.568-4T>C	ENSP00000422846.1:n.568-4T>C
ENST00000478180.6:c.568-4T>C	ENSP00000426059.1:n.568-4T>C
ENST00000507747.1:c.434+4296T>C
ENST00000508775.5:c.568-4T>C	ENSP00000426455.1:n.568-4T>C
ENST00000510083.1:n.2007-4T>C
ENST00000611959.2:c.*356-4T>C	ENSP00000480244.2:n.*356-4T>C
ENST00000620173.4:c.718-4T>C	ENSP00000482755.1:n.718-4T>C
ENST00000620173.5:c.454-4T>C	ENSP00000482755.2:n.454-4T>C
ENST00000682498.1:n.2686-4T>C
ENST00000682774.1:c.*409-4T>C	ENSP00000507399.1:n.*409-4T>C
ENST00000683770.1:c.322-4T>C	ENSP00000507710.1:n.322-4T>C
ENST00000683968.1:n.3060-4T>C
ENST00000684236.1:c.292-4T>C	ENSP00000508128.1:n.292-4T>C
XM_017011397.1:c.454-4T>C	XP_016866886.1:n.454-4T>C
XM_017011398.1:c.292-4T>C	XP_016866887.1:n.292-4T>C
XM_017011399.1:c.*33-4T>C	XP_016866888.1:n.*33-4T>C
XM_024446575.1:c.292-4T>C	XP_024302343.1:n.292-4T>C
XM_024446576.1:c.292-4T>C	XP_024302344.1:n.292-4T>C