Canonical Allele Identifier: CA916081809

Gene: PALB2

Linked Data

• ClinVar Variation Id: 848156
• ClinVar RCV Id: RCV001051853
• dbSNP Id: rs1966989564

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635385del , CM000678.2:g.23635385del	GRCh38
NC_000016.9:g.23646706del , CM000678.1:g.23646706del	GRCh37
NC_000016.8:g.23554207del	NCBI36
NG_007406.1:g.10973del , LRG_308:g.10973del

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.1167del	ENSP00000460666.3:p.Pro390LeufsTer?
ENST00000565038.2:c.211+2465del	ENSP00000459882.2:n.211+2465del
ENST00000566069.6:c.1161del	ENSP00000459237.2:p.Pro388LeufsTer?
ENST00000697377.2:c.1167del	ENSP00000513286.2:p.Pro390LeufsTer?
ENST00000697379.2:c.1167del	ENSP00000513287.2:p.Pro390LeufsTer?
ENST00000561514.2:c.276del	ENSP00000460666.2:p.Pro93LeufsTer?
ENST00000697374.1:c.276del	ENSP00000513284.1:p.Pro93LeufsTer?
ENST00000697375.1:n.2508del
ENST00000697376.1:c.276del	ENSP00000513285.1:p.Pro93LeufsTer?
ENST00000697377.1:c.276del	ENSP00000513286.1:p.Pro93LeufsTer?
ENST00000697378.1:n.1681del
ENST00000697379.1:c.276del	ENSP00000513287.1:p.Pro93LeufsTer?
ENST00000697382.1:c.276del	ENSP00000513288.1:p.Pro93LeufsTer?
ENST00000697383.1:c.48+5725del	ENSP00000513289.1:n.48+5725del
ENST00000697384.1:n.1315del
ENST00000261584.9:c.1161del MANE Select	ENSP00000261584.4:p.Pro388LeufsTer?
ENST00000261584.8:c.1161del	ENSP00000261584.4:p.Pro388LeufsTer?
ENST00000565038.1:c.86+2465del
ENST00000568219.5:c.276del	ENSP00000454703.2:p.Pro93LeufsTer?
NM_024675.3:c.1161del , LRG_308t1:c.1161del	NP_078951.2:p.Pro388LeufsTer?
XM_011545946.1:c.1167del	XP_011544248.1:p.Pro390LeufsTer?
XM_011545947.1:c.1167del	XP_011544249.1:p.Pro390LeufsTer?
XM_011545948.1:c.276del	XP_011544250.1:p.Pro93LeufsTer?
XR_950851.1:n.1957del
XM_011545946.2:c.1167del	XP_011544248.1:p.Pro390LeufsTer?
XM_011545947.2:c.1167del	XP_011544249.1:p.Pro390LeufsTer?
XM_011545948.2:c.276del	XP_011544250.1:p.Pro93LeufsTer?
XM_017023671.1:c.1167del	XP_016879160.1:p.Pro390LeufsTer?
XM_017023672.2:c.1161del	XP_016879161.1:p.Pro388LeufsTer?
XM_017023673.2:c.1161del	XP_016879162.1:p.Pro388LeufsTer?
NM_024675.4:c.1161del MANE Select	NP_078951.2:p.Pro388LeufsTer?