Canonical Allele Identifier: CA395132296
Gene: PALB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23635220A>T , CM000678.2:g.23635220A>T GRCh38
NC_000016.9:g.23646541A>T , CM000678.1:g.23646541A>T GRCh37
NC_000016.8:g.23554042A>T NCBI36
NG_007406.1:g.11138T>A , LRG_308:g.11138T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.1332T>A ENSP00000460666.3:p.Asn444Lys
ENST00000565038.2:c.211+2630T>A ENSP00000459882.2:n.211+2630T>A
ENST00000566069.6:c.1326T>A ENSP00000459237.2:p.Asn442Lys
ENST00000697377.2:c.1332T>A ENSP00000513286.2:p.Asn444Lys
ENST00000697379.2:c.1332T>A ENSP00000513287.2:p.Asn444Lys
ENST00000561514.2:c.441T>A ENSP00000460666.2:p.Asn147Lys
ENST00000697374.1:c.441T>A ENSP00000513284.1:p.Asn147Lys
ENST00000697375.1:n.2673T>A
ENST00000697376.1:c.441T>A ENSP00000513285.1:p.Asn147Lys
ENST00000697377.1:c.441T>A ENSP00000513286.1:p.Asn147Lys
ENST00000697378.1:n.1846T>A
ENST00000697379.1:c.441T>A ENSP00000513287.1:p.Asn147Lys
ENST00000697382.1:c.441T>A ENSP00000513288.1:p.Asn147Lys
ENST00000697383.1:c.48+5890T>A ENSP00000513289.1:n.48+5890T>A
ENST00000697384.1:n.1480T>A
ENST00000261584.9:c.1326T>A MANE Select ENSP00000261584.4:p.Asn442Lys
ENST00000261584.8:c.1326T>A ENSP00000261584.4:p.Asn442Lys
ENST00000565038.1:c.86+2630T>A
ENST00000568219.5:c.441T>A ENSP00000454703.2:p.Asn147Lys
NM_024675.3:c.1326T>A , LRG_308t1:c.1326T>A NP_078951.2:p.Asn442Lys
XM_011545946.1:c.1332T>A XP_011544248.1:p.Asn444Lys
XM_011545947.1:c.1332T>A XP_011544249.1:p.Asn444Lys
XM_011545948.1:c.441T>A XP_011544250.1:p.Asn147Lys
XR_950851.1:n.2122T>A
XM_011545946.2:c.1332T>A XP_011544248.1:p.Asn444Lys
XM_011545947.2:c.1332T>A XP_011544249.1:p.Asn444Lys
XM_011545948.2:c.441T>A XP_011544250.1:p.Asn147Lys
XM_017023671.1:c.1332T>A XP_016879160.1:p.Asn444Lys
XM_017023672.2:c.1326T>A XP_016879161.1:p.Asn442Lys
XM_017023673.2:c.1326T>A XP_016879162.1:p.Asn442Lys
NM_024675.4:c.1326T>A MANE Select NP_078951.2:p.Asn442Lys