Canonical Allele Identifier: CA1211556413
Gene: RNASEL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182586017T= , CM000663.2:g.182586017T= GRCh38
NC_000001.10:g.182555152T= , CM000663.1:g.182555152T= GRCh37
NC_000001.9:g.180821775T= NCBI36
NG_009024.2:g.5957A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367559.7:c.790A= MANE Select ENSP00000356530.3:p.Ile264=
ENST00000539397.1:c.790A= ENSP00000440844.1:p.Ile264=
NM_021133.3:c.790A= NP_066956.1:p.Ile264=
XM_005245411.2:c.790A= XP_005245468.1:p.Ile264=
XR_001737359.1:n.1073A=
XR_001737360.1:n.1073A=
NM_021133.4:c.790A= MANE Select NP_066956.1:p.Ile264=