Canonical Allele Identifier: CA1211556399
Gene: RNASEL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182585982T= , CM000663.2:g.182585982T= GRCh38
NC_000001.10:g.182555117T= , CM000663.1:g.182555117T= GRCh37
NC_000001.9:g.180821740T= NCBI36
NG_009024.2:g.5992A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367559.7:c.825A= MANE Select ENSP00000356530.3:p.Thr275=
ENST00000539397.1:c.825A= ENSP00000440844.1:p.Thr275=
NM_021133.3:c.825A= NP_066956.1:p.Thr275=
XM_005245411.2:c.825A= XP_005245468.1:p.Thr275=
XR_001737359.1:n.1108A=
XR_001737360.1:n.1108A=
NM_021133.4:c.825A= MANE Select NP_066956.1:p.Thr275=