Canonical Allele Identifier: CA4095206

Gene: RNASET2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.166956167G>A , CM000668.2:g.166956167G>A	GRCh38
NC_000006.11:g.167369655G>A , CM000668.1:g.167369655G>A	GRCh37
NC_000006.10:g.167289645G>A	NCBI36
NG_016280.1:g.5423C>T
NG_016280.2:g.5423C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003730.6:c.16C>T MANE Select	NP_003721.2:p.Leu6=
ENST00000508775.6:c.16C>T MANE Select	ENSP00000426455.2:p.Leu6=
NM_003730.4:c.16C>T	NP_003721.2:p.Leu6=
NM_003730.5:c.16C>T	NP_003721.2:p.Leu6=
ENST00000028008.9:c.16C>T	ENSP00000028008.5:p.Leu6=
ENST00000358165.7:n.243+782C>T
ENST00000366855.10:c.-232C>T	ENSP00000424947.1:n.-232C>T
ENST00000421787.5:c.16C>T	ENSP00000390833.1:p.Leu6=
ENST00000476238.6:c.16C>T	ENSP00000422846.1:p.Leu6=
ENST00000478180.6:c.16C>T	ENSP00000426059.1:p.Leu6=
ENST00000508775.5:c.16C>T	ENSP00000426455.1:p.Leu6=
ENST00000611959.1:c.16C>T	ENSP00000480244.1:p.Leu6=
ENST00000611959.2:c.16C>T	ENSP00000480244.2:p.Leu6=
ENST00000620173.4:c.16C>T	ENSP00000482755.1:p.Leu6=
ENST00000620173.5:c.16C>T	ENSP00000482755.2:p.Leu6=
ENST00000682774.1:c.16C>T	ENSP00000507399.1:p.Leu6=
ENST00000683158.1:n.16C>T
ENST00000683333.1:n.401C>T
ENST00000683770.1:c.16C>T	ENSP00000507710.1:p.Leu6=
ENST00000684236.1:c.-349C>T	ENSP00000508128.1:n.-349C>T
XM_017011397.1:c.-243C>T	XP_016866886.1:n.-243C>T
XM_017011398.1:c.-205C>T	XP_016866887.1:n.-205C>T
XM_017011399.1:c.16C>T	XP_016866888.1:p.Leu6=
XM_024446575.1:c.-366C>T	XP_024302343.1:n.-366C>T
XM_024446576.1:c.-349C>T	XP_024302344.1:n.-349C>T