Canonical Allele Identifier: CA151912155

Gene: RNASET2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.166956337G>A , CM000668.2:g.166956337G>A	GRCh38
NC_000006.11:g.167369825G>A , CM000668.1:g.167369825G>A	GRCh37
NC_000006.10:g.167289815G>A	NCBI36
NG_016280.1:g.5253C>T
NG_016280.2:g.5253C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003730.6:c.-155C>T MANE Select	NP_003721.2:n.-155C>T
ENST00000508775.6:c.-155C>T MANE Select	ENSP00000426455.2:n.-155C>T
NM_003730.4:c.-155C>T	NP_003721.2:n.-155C>T
NM_003730.5:c.-155C>T	NP_003721.2:n.-155C>T
ENST00000028008.9:c.-155C>T	ENSP00000028008.5:n.-155C>T
ENST00000358165.7:n.243+612C>T
ENST00000366855.10:c.-402C>T	ENSP00000424947.1:n.-402C>T
ENST00000421787.5:c.-155C>T	ENSP00000390833.1:n.-155C>T
ENST00000476238.6:c.-9-146C>T	ENSP00000422846.1:n.-9-146C>T
ENST00000478180.6:c.-9-146C>T	ENSP00000426059.1:n.-9-146C>T
ENST00000508775.5:c.-155C>T	ENSP00000426455.1:n.-155C>T
ENST00000611959.1:c.-155C>T	ENSP00000480244.1:n.-155C>T
ENST00000611959.2:c.-155C>T	ENSP00000480244.2:n.-155C>T
ENST00000620173.4:c.-155C>T	ENSP00000482755.1:n.-155C>T
ENST00000620173.5:c.-155C>T	ENSP00000482755.2:n.-155C>T
ENST00000683333.1:n.231C>T
ENST00000683770.1:c.-155C>T	ENSP00000507710.1:n.-155C>T
XM_017011398.1:c.-375C>T	XP_016866887.1:n.-375C>T
XM_017011399.1:c.-155C>T	XP_016866888.1:n.-155C>T
XM_024446575.1:c.-536C>T	XP_024302343.1:n.-536C>T