Canonical Allele Identifier: CA1211556504
Gene: RNASEL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182586282A= , CM000663.2:g.182586282A= GRCh38
NC_000001.10:g.182555417A= , CM000663.1:g.182555417A= GRCh37
NC_000001.9:g.180822040A= NCBI36
NG_009024.2:g.5692T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367559.7:c.525T= MANE Select ENSP00000356530.3:p.Ala175=
ENST00000539397.1:c.525T= ENSP00000440844.1:p.Ala175=
NM_021133.3:c.525T= NP_066956.1:p.Ala175=
XM_005245411.2:c.525T= XP_005245468.1:p.Ala175=
XR_001737359.1:n.808T=
XR_001737360.1:n.808T=
NM_021133.4:c.525T= MANE Select NP_066956.1:p.Ala175=