Canonical Allele Identifier: CA1211556510
Gene: RNASEL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182586306_182586307delinsTC , CM000663.2:g.182586306_182586307delinsTC GRCh38
NC_000001.10:g.182555441_182555442delinsTC , CM000663.1:g.182555441_182555442delinsTC GRCh37
NC_000001.9:g.180822064_180822065delinsTC NCBI36
NG_009024.2:g.5667_5668delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000367559.7:c.500_501delinsGA MANE Select ENSP00000356530.3:p.Gly167=
ENST00000539397.1:c.500_501delinsGA ENSP00000440844.1:p.Gly167=
NM_021133.3:c.500_501delinsGA NP_066956.1:p.Gly167=
XM_005245411.2:c.500_501delinsGA XP_005245468.1:p.Gly167=
XR_001737359.1:n.783_784delinsGA
XR_001737360.1:n.783_784delinsGA
NM_021133.4:c.500_501delinsGA MANE Select NP_066956.1:p.Gly167=
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Search 100 bp 3'