Canonical Allele Identifier: CA1149049168

Gene: RNASEL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.182586299T= , CM000663.2:g.182586299T=	GRCh38
NC_000001.10:g.182555434T= , CM000663.1:g.182555434T=	GRCh37
NC_000001.9:g.180822057T=	NCBI36
NG_009024.2:g.5675A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367559.7:c.508A= MANE Select	ENSP00000356530.3:p.Thr170=
ENST00000539397.1:c.508A=	ENSP00000440844.1:p.Thr170=
NM_021133.3:c.508A=	NP_066956.1:p.Thr170=
XM_005245411.2:c.508A=	XP_005245468.1:p.Thr170=
XR_001737359.1:n.791A=
XR_001737360.1:n.791A=
NM_021133.4:c.508A= MANE Select	NP_066956.1:p.Thr170=