Canonical Allele Identifier: CA1211556450
Gene: RNASEL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182586119C= , CM000663.2:g.182586119C= GRCh38
NC_000001.10:g.182555254C= , CM000663.1:g.182555254C= GRCh37
NC_000001.9:g.180821877C= NCBI36
NG_009024.2:g.5855G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367559.7:c.688G= MANE Select ENSP00000356530.3:p.Ala230=
ENST00000539397.1:c.688G= ENSP00000440844.1:p.Ala230=
NM_021133.3:c.688G= NP_066956.1:p.Ala230=
XM_005245411.2:c.688G= XP_005245468.1:p.Ala230=
XR_001737359.1:n.971G=
XR_001737360.1:n.971G=
NM_021133.4:c.688G= MANE Select NP_066956.1:p.Ala230=