Canonical Allele Identifier: CA1680137228

Gene: RNASET2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.166949985C= , CM000668.2:g.166949985C=	GRCh38
NC_000006.11:g.167363473C= , CM000668.1:g.167363473C=	GRCh37
NC_000006.10:g.167283463C=	NCBI36
NG_016280.1:g.11605G=
NG_016280.2:g.11605G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003730.6:c.148-1360G= MANE Select	NP_003721.2:n.148-1360G=
ENST00000508775.6:c.148-1360G= MANE Select	ENSP00000426455.2:n.148-1360G=
NM_003730.4:c.148-1360G=	NP_003721.2:n.148-1360G=
NM_003730.5:c.148-1360G=	NP_003721.2:n.148-1360G=
ENST00000028008.9:c.148-1360G=	ENSP00000028008.5:n.148-1360G=
ENST00000358165.7:n.244-6896G=
ENST00000366855.10:c.34-1360G=	ENSP00000424947.1:n.34-1360G=
ENST00000421787.5:c.148-1360G=	ENSP00000390833.1:n.148-1360G=
ENST00000476238.6:c.148-1360G=	ENSP00000422846.1:n.148-1360G=
ENST00000478180.6:c.148-1360G=	ENSP00000426059.1:n.148-1360G=
ENST00000496851.6:n.48-1360G=
ENST00000499370.6:n.1094-1360G=
ENST00000507747.1:c.90-1360G=
ENST00000508775.5:c.148-1360G=	ENSP00000426455.1:n.148-1360G=
ENST00000611959.1:c.148-1360G=	ENSP00000480244.1:n.148-1360G=
ENST00000611959.2:c.147+2503G=	ENSP00000480244.2:n.147+2503G=
ENST00000620173.4:c.148-1360G=	ENSP00000482755.1:n.148-1360G=
ENST00000620173.5:c.147+2503G=	ENSP00000482755.2:n.147+2503G=
ENST00000682774.1:c.148-1360G=	ENSP00000507399.1:n.148-1360G=
ENST00000683158.1:n.309-1360G=
ENST00000683770.1:c.86+6112G=	ENSP00000507710.1:n.86+6112G=
ENST00000683968.1:n.2695+2503G=
ENST00000684236.1:c.-74+2503G=	ENSP00000508128.1:n.-74+2503G=
XM_017011397.1:c.34-1360G=	XP_016866886.1:n.34-1360G=
XM_017011398.1:c.-74+2503G=	XP_016866887.1:n.-74+2503G=
XM_017011399.1:c.148-1360G=	XP_016866888.1:n.148-1360G=
XM_024446575.1:c.-74+2503G=	XP_024302343.1:n.-74+2503G=
XM_024446576.1:c.-74+2503G=	XP_024302344.1:n.-74+2503G=