Canonical Allele Identifier: CA1211556524
Gene: RNASEL HGNC NCBI

Linked Data

dbSNP Id: rs1661595834

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182586333dup , CM000663.2:g.182586333dup GRCh38
NC_000001.10:g.182555468dup , CM000663.1:g.182555468dup GRCh37
NC_000001.9:g.180822091dup NCBI36
NG_009024.2:g.5642dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367559.7:c.475dup MANE Select ENSP00000356530.3:p.Glu159GlyfsTer19
ENST00000539397.1:c.475dup ENSP00000440844.1:p.Glu159GlyfsTer19
NM_021133.3:c.475dup NP_066956.1:p.Glu159GlyfsTer19
XM_005245411.2:c.475dup XP_005245468.1:p.Glu159GlyfsTer19
XR_001737359.1:n.758dup
XR_001737360.1:n.758dup
NM_021133.4:c.475dup MANE Select NP_066956.1:p.Glu159GlyfsTer19