Canonical Allele Identifier: CA1148449337
Gene: RNASEL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182586333_182586336delinsCTTT , CM000663.2:g.182586333_182586336delinsCTTT GRCh38
NC_000001.10:g.182555468_182555471delinsCTTT , CM000663.1:g.182555468_182555471delinsCTTT GRCh37
NC_000001.9:g.180822091_180822094delinsCTTT NCBI36
NG_009024.2:g.5638_5641delinsAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367559.7:c.471_474delinsAAAG MANE Select ENSP00000356530.3:p.Thr157=
ENST00000539397.1:c.471_474delinsAAAG ENSP00000440844.1:p.Thr157=
NM_021133.3:c.471_474delinsAAAG NP_066956.1:p.Thr157=
XM_005245411.2:c.471_474delinsAAAG XP_005245468.1:p.Thr157=
XR_001737359.1:n.754_757delinsAAAG
XR_001737360.1:n.754_757delinsAAAG
NM_021133.4:c.471_474delinsAAAG MANE Select NP_066956.1:p.Thr157=
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