Canonical Allele Identifier: CA10626447

Gene: RNASET2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.166956214T>C , CM000668.2:g.166956214T>C	GRCh38
NC_000006.11:g.167369702T>C , CM000668.1:g.167369702T>C	GRCh37
NC_000006.10:g.167289692T>C	NCBI36
NG_016280.1:g.5376A>G
NG_016280.2:g.5376A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003730.6:c.-32A>G MANE Select	NP_003721.2:n.-32A>G
ENST00000508775.6:c.-32A>G MANE Select	ENSP00000426455.2:n.-32A>G
NM_003730.4:c.-32A>G	NP_003721.2:n.-32A>G
NM_003730.5:c.-32A>G	NP_003721.2:n.-32A>G
ENST00000028008.9:c.-32A>G	ENSP00000028008.5:n.-32A>G
ENST00000358165.7:n.243+735A>G
ENST00000366855.10:c.-279A>G	ENSP00000424947.1:n.-279A>G
ENST00000421787.5:c.-32A>G	ENSP00000390833.1:n.-32A>G
ENST00000476238.6:c.-9-23A>G	ENSP00000422846.1:n.-9-23A>G
ENST00000478180.6:c.-9-23A>G	ENSP00000426059.1:n.-9-23A>G
ENST00000508775.5:c.-32A>G	ENSP00000426455.1:n.-32A>G
ENST00000611959.1:c.-32A>G	ENSP00000480244.1:n.-32A>G
ENST00000611959.2:c.-32A>G	ENSP00000480244.2:n.-32A>G
ENST00000620173.4:c.-32A>G	ENSP00000482755.1:n.-32A>G
ENST00000620173.5:c.-32A>G	ENSP00000482755.2:n.-32A>G
ENST00000682774.1:c.-32A>G	ENSP00000507399.1:n.-32A>G
ENST00000683333.1:n.354A>G
ENST00000683770.1:c.-32A>G	ENSP00000507710.1:n.-32A>G
XM_017011397.1:c.-290A>G	XP_016866886.1:n.-290A>G
XM_017011398.1:c.-252A>G	XP_016866887.1:n.-252A>G
XM_017011399.1:c.-32A>G	XP_016866888.1:n.-32A>G
XM_024446575.1:c.-413A>G	XP_024302343.1:n.-413A>G