Canonical Allele Identifier: CA294510
Gene: PALB2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 126696

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23623045_23623046del , CM000678.2:g.23623045_23623046del GRCh38
NC_000016.9:g.23634366_23634367del , CM000678.1:g.23634366_23634367del GRCh37
NC_000016.8:g.23541867_23541868del NCBI36
NG_007406.1:g.23313_23314del , LRG_308:g.23313_23314del

Transcript Alleles

HGVS Amino-acid change
NM_024675.3:c.2920_2921del , LRG_308t1:c.2920_2921del NP_078951.2:p.Lys974GlufsTer5
XM_011545946.1:c.2926_2927del XP_011544248.1:p.Lys976GlufsTer5
XM_011545947.1:c.2926_2927del XP_011544249.1:p.Lys976GlufsTer5
XM_011545948.1:c.2035_2036del XP_011544250.1:p.Lys679GlufsTer5
XR_950851.1:n.3716_3717del
XM_011545946.2:c.2926_2927del XP_011544248.1:p.Lys976GlufsTer5
XM_011545947.2:c.2926_2927del XP_011544249.1:p.Lys976GlufsTer5
XM_011545948.2:c.2035_2036del XP_011544250.1:p.Lys679GlufsTer5
XM_017023671.1:c.2926_2927del XP_016879160.1:p.Lys976GlufsTer5
XM_017023672.2:c.2920_2921del XP_016879161.1:p.Lys974GlufsTer5
XM_017023673.2:c.2920_2921del XP_016879162.1:p.Lys974GlufsTer5
ENST00000261584.8:c.2920_2921del ENSP00000261584.4:p.Lys974GlufsTer5
ENST00000568219.5:c.2035_2036del ENSP00000454703.2:p.Lys679GlufsTer5