Canonical Allele Identifier: CA2580081685
Community Standard Title: NM_032199.3(ARID5B):c.1302del (p.Asn434LysfsTer?)
Gene: ARID5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62085804del , CM000672.2:g.62085804del GRCh38
NC_000010.10:g.63845563del , CM000672.1:g.63845563del GRCh37
NC_000010.9:g.63515569del NCBI36
NG_030027.1:g.189551del

Transcript Alleles

HGVS Amino-acid Change
NM_032199.3:c.1302del MANE Select NP_115575.1:p.Asn434LysfsTer?
ENST00000279873.12:c.1302del MANE Select ENSP00000279873.7:p.Asn434LysfsTer?
NM_001244638.1:c.573del NP_001231567.1:p.Asn191LysfsTer?
NM_001244638.2:c.573del NP_001231567.1:p.Asn191LysfsTer?
NM_032199.2:c.1302del NP_115575.1:p.Asn434LysfsTer?
ENST00000279873.11:c.1302del ENSP00000279873.7:p.Asn434LysfsTer?
ENST00000309334.5:c.573del ENSP00000308862.5:p.Asn191LysfsTer?
ENST00000681100.1:c.1278del ENSP00000506119.1:p.Asn426LysfsTer?
XM_011540262.1:c.1071del XP_011538564.1:p.Asn357LysfsTer?
XM_024448230.1:c.735del XP_024303998.1:p.Asn245LysfsTer?
XM_024448231.1:c.-175del XP_024303999.1:n.-175del