Canonical Allele Identifier: CA2610892755
Gene: RBM20 HGNC NCBI

Linked Data

gnomAD v4: 10-110812218-TGGGTG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812226_110812230del , CM000672.2:g.110812226_110812230del GRCh38
NC_000010.10:g.112571984_112571988del , CM000672.1:g.112571984_112571988del GRCh37
NC_000010.9:g.112561974_112561978del NCBI36
NG_021177.1:g.172830_172834del , LRG_382:g.172830_172834del

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.1881-52_1881-48del MANE Select ENSP00000358532.3:n.1881-52_1881-48del
ENST00000369519.3:c.1881-52_1881-48del ENSP00000358532.3:n.1881-52_1881-48del
NM_001134363.2:c.1881-52_1881-48del NP_001127835.2:n.1881-52_1881-48del
XM_011539697.1:c.1497-52_1497-48del XP_011537999.1:n.1497-52_1497-48del
XM_017016103.2:c.1716-52_1716-48del XP_016871592.1:n.1716-52_1716-48del
XM_017016104.2:c.1497-52_1497-48del XP_016871593.1:n.1497-52_1497-48del
NM_001134363.3:c.1881-52_1881-48del MANE Select NP_001127835.2:n.1881-52_1881-48del
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