Canonical Allele Identifier: CA169555
Gene: PALB2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 126734
dbSNP Id: rs180177135

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23607891del , CM000678.2:g.23607891del GRCh38
NC_000016.9:g.23619212del , CM000678.1:g.23619212del GRCh37
NC_000016.8:g.23526713del NCBI36
NG_007406.1:g.38467del , LRG_308:g.38467del

Transcript Alleles

HGVS Amino-acid change
NM_024675.3:c.3323del , LRG_308t1:c.3323del NP_078951.2:p.Tyr1108SerfsTer16
XM_011545946.1:c.3329del XP_011544248.1:p.Tyr1110SerfsTer16
XM_011545947.1:c.3208-4222del XP_011544249.1:p.=
XM_011545948.1:c.2438del XP_011544250.1:p.Tyr813SerfsTer16
XR_950851.1:n.4031del
XM_011545946.2:c.3329del XP_011544248.1:p.Tyr1110SerfsTer16
XM_011545947.2:c.3208-4222del XP_011544249.1:p.=
XM_011545948.2:c.2438del XP_011544250.1:p.Tyr813SerfsTer16
XM_017023671.1:c.3120-4222del XP_016879160.1:p.=
XM_017023672.2:c.3114-4222del XP_016879161.1:p.=
XM_017023673.2:c.3202-4222del XP_016879162.1:p.=
ENST00000261584.8:c.3323del ENSP00000261584.4:p.Tyr1108SerfsTer16
ENST00000566069.5:n.117-4222del
ENST00000568219.5:c.2438del ENSP00000454703.2:p.Tyr813SerfsTer16