Canonical Allele Identifier: CA1139659945

Gene: RNASET2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.166956403C>T , CM000668.2:g.166956403C>T	GRCh38
NC_000006.11:g.167369891C>T , CM000668.1:g.167369891C>T	GRCh37
NC_000006.10:g.167289881C>T	NCBI36
NG_016280.1:g.5187G>A
NG_016280.2:g.5187G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003730.6:c.-221G>A MANE Select	NP_003721.2:n.-221G>A
ENST00000508775.6:c.-221G>A MANE Select	ENSP00000426455.2:n.-221G>A
NM_003730.4:c.-221G>A	NP_003721.2:n.-221G>A
NM_003730.5:c.-221G>A	NP_003721.2:n.-221G>A
ENST00000028008.9:c.-221G>A	ENSP00000028008.5:n.-221G>A
ENST00000358165.7:n.243+546G>A
ENST00000366855.10:c.-468G>A	ENSP00000424947.1:n.-468G>A
ENST00000421787.5:c.-221G>A	ENSP00000390833.1:n.-221G>A
ENST00000476238.6:c.-9-212G>A	ENSP00000422846.1:n.-9-212G>A
ENST00000478180.6:c.-9-212G>A	ENSP00000426059.1:n.-9-212G>A
ENST00000508775.5:c.-221G>A	ENSP00000426455.1:n.-221G>A
ENST00000611959.1:c.-221G>A	ENSP00000480244.1:n.-221G>A
ENST00000611959.2:c.-221G>A	ENSP00000480244.2:n.-221G>A
ENST00000620173.4:c.-221G>A	ENSP00000482755.1:n.-221G>A
ENST00000683333.1:n.165G>A
ENST00000683770.1:c.-221G>A	ENSP00000507710.1:n.-221G>A
XM_017011398.1:c.-441G>A	XP_016866887.1:n.-441G>A
XM_017011399.1:c.-221G>A	XP_016866888.1:n.-221G>A
XM_024446575.1:c.-602G>A	XP_024302343.1:n.-602G>A