Canonical Allele Identifier: CA2695222996

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641145del , CM000678.2:g.23641145del	GRCh38
NC_000016.9:g.23652466del , CM000678.1:g.23652466del	GRCh37
NC_000016.8:g.23559967del	NCBI36
NG_007406.1:g.5215del , LRG_308:g.5215del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-838del	ENSP00000460666.3:n.-838del
ENST00000565038.2:c.15del	ENSP00000459882.2:p.Lys7SerfsTer11
ENST00000566069.6:c.15del	ENSP00000459237.2:p.Lys7SerfsTer11
ENST00000697377.2:c.-225del	ENSP00000513286.2:n.-225del
ENST00000697379.2:c.-131del	ENSP00000513287.2:n.-131del
ENST00000561514.2:c.-1729del	ENSP00000460666.2:n.-1729del
ENST00000697374.1:c.-1320del	ENSP00000513284.1:n.-1320del
ENST00000697376.1:c.-1041del	ENSP00000513285.1:n.-1041del
ENST00000697377.1:c.-1116del	ENSP00000513286.1:n.-1116del
ENST00000697379.1:c.-1022del	ENSP00000513287.1:n.-1022del
ENST00000697382.1:c.-1780del	ENSP00000513288.1:n.-1780del
ENST00000697383.1:c.15del	ENSP00000513289.1:p.Lys7SerfsTer22
ENST00000697384.1:n.169del
ENST00000261584.9:c.15del MANE Select	ENSP00000261584.4:p.Lys7SerfsTer11
ENST00000261584.8:c.15del	ENSP00000261584.4:p.Lys7SerfsTer11
ENST00000567003.1:n.159del
ENST00000568219.5:c.-854del	ENSP00000454703.2:n.-854del
NM_024675.3:c.15del , LRG_308t1:c.15del	NP_078951.2:p.Lys7SerfsTer11
XM_011545948.1:c.-1005del	XP_011544250.1:n.-1005del
XM_011545946.2:c.-838del	XP_011544248.1:n.-838del
XM_011545947.2:c.-838del	XP_011544249.1:n.-838del
XM_011545948.2:c.-1005del	XP_011544250.1:n.-1005del
XM_017023671.1:c.-838del	XP_016879160.1:n.-838del
XM_017023672.2:c.15del	XP_016879161.1:p.Lys7SerfsTer11
XM_017023673.2:c.15del	XP_016879162.1:p.Lys7SerfsTer11
NM_024675.4:c.15del MANE Select	NP_078951.2:p.Lys7SerfsTer11