Canonical Allele Identifier: CA2213436432
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23641128_23641129delinsGC , CM000678.2:g.23641128_23641129delinsGC GRCh38
NC_000016.9:g.23652449_23652450delinsGC , CM000678.1:g.23652449_23652450delinsGC GRCh37
NC_000016.8:g.23559950_23559951delinsGC NCBI36
NG_007406.1:g.5229_5230delinsGC , LRG_308:g.5229_5230delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.-824_-823delinsGC ENSP00000460666.3:n.-824_-823delinsGC
ENST00000565038.2:c.29_30delinsGC ENSP00000459882.2:p.Ser10=
ENST00000566069.6:c.29_30delinsGC ENSP00000459237.2:p.Ser10=
ENST00000697377.2:c.-211_-210delinsGC ENSP00000513286.2:n.-211_-210delinsGC
ENST00000697379.2:c.-117_-116delinsGC ENSP00000513287.2:n.-117_-116delinsGC
ENST00000561514.2:c.-1715_-1714delinsGC ENSP00000460666.2:n.-1715_-1714delinsGC
ENST00000697374.1:c.-1306_-1305delinsGC ENSP00000513284.1:n.-1306_-1305delinsGC
ENST00000697376.1:c.-1027_-1026delinsGC ENSP00000513285.1:n.-1027_-1026delinsGC
ENST00000697377.1:c.-1102_-1101delinsGC ENSP00000513286.1:n.-1102_-1101delinsGC
ENST00000697379.1:c.-1008_-1007delinsGC ENSP00000513287.1:n.-1008_-1007delinsGC
ENST00000697382.1:c.-1766_-1765delinsGC ENSP00000513288.1:n.-1766_-1765delinsGC
ENST00000697383.1:c.29_30delinsGC ENSP00000513289.1:p.Ser10=
ENST00000697384.1:n.183_184delinsGC
ENST00000261584.9:c.29_30delinsGC MANE Select ENSP00000261584.4:p.Ser10=
ENST00000261584.8:c.29_30delinsGC ENSP00000261584.4:p.Ser10=
ENST00000567003.1:n.173_174delinsGC
ENST00000568219.5:c.-840_-839delinsGC ENSP00000454703.2:n.-840_-839delinsGC
NM_024675.3:c.29_30delinsGC , LRG_308t1:c.29_30delinsGC NP_078951.2:p.Ser10=
XM_011545948.1:c.-991_-990delinsGC XP_011544250.1:n.-991_-990delinsGC
XM_011545946.2:c.-824_-823delinsGC XP_011544248.1:n.-824_-823delinsGC
XM_011545947.2:c.-824_-823delinsGC XP_011544249.1:n.-824_-823delinsGC
XM_011545948.2:c.-991_-990delinsGC XP_011544250.1:n.-991_-990delinsGC
XM_017023671.1:c.-824_-823delinsGC XP_016879160.1:n.-824_-823delinsGC
XM_017023672.2:c.29_30delinsGC XP_016879161.1:p.Ser10=
XM_017023673.2:c.29_30delinsGC XP_016879162.1:p.Ser10=
NM_024675.4:c.29_30delinsGC MANE Select NP_078951.2:p.Ser10=