Canonical Allele Identifier: CA915949191

Gene: PALB2

Linked Data

• ClinVar Variation Id: 665364
• ClinVar RCV Id: RCV000823630 ; RCV002415945
• dbSNP Id: rs1597090596

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23630193del , CM000678.2:g.23630193del	GRCh38
NC_000016.9:g.23641514del , CM000678.1:g.23641514del	GRCh37
NC_000016.8:g.23549015del	NCBI36
NG_007406.1:g.16169del , LRG_308:g.16169del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1971del	ENSP00000460666.3:p.Pro658GlnfsTer4
ENST00000565038.2:c.212-914del	ENSP00000459882.2:n.212-914del
ENST00000566069.6:c.1965del	ENSP00000459237.2:p.Pro656GlnfsTer4
ENST00000697377.2:c.1971del	ENSP00000513286.2:p.Pro658GlnfsTer4
ENST00000697379.2:c.1971del	ENSP00000513287.2:p.Pro658GlnfsTer4
ENST00000561514.2:c.1080del	ENSP00000460666.2:p.Pro361GlnfsTer4
ENST00000697374.1:c.1080del	ENSP00000513284.1:p.Pro361GlnfsTer4
ENST00000697375.1:n.3312del
ENST00000697376.1:c.1080del	ENSP00000513285.1:p.Pro361GlnfsTer4
ENST00000697377.1:c.1080del	ENSP00000513286.1:p.Pro361GlnfsTer4
ENST00000697378.1:n.2485del
ENST00000697379.1:c.1080del	ENSP00000513287.1:p.Pro361GlnfsTer4
ENST00000697380.1:n.893del
ENST00000697381.1:n.660del
ENST00000697382.1:c.1080del	ENSP00000513288.1:p.Pro361GlnfsTer4
ENST00000697383.1:c.49-914del	ENSP00000513289.1:n.49-914del
ENST00000697384.1:n.2119del
ENST00000261584.9:c.1965del MANE Select	ENSP00000261584.4:p.Pro656GlnfsTer4
ENST00000261584.8:c.1965del	ENSP00000261584.4:p.Pro656GlnfsTer4
ENST00000565038.1:c.87-914del
ENST00000568219.5:c.1080del	ENSP00000454703.2:p.Pro361GlnfsTer4
NM_024675.3:c.1965del , LRG_308t1:c.1965del	NP_078951.2:p.Pro656GlnfsTer4
XM_011545946.1:c.1971del	XP_011544248.1:p.Pro658GlnfsTer4
XM_011545947.1:c.1971del	XP_011544249.1:p.Pro658GlnfsTer4
XM_011545948.1:c.1080del	XP_011544250.1:p.Pro361GlnfsTer4
XR_950851.1:n.2761del
XM_011545946.2:c.1971del	XP_011544248.1:p.Pro658GlnfsTer4
XM_011545947.2:c.1971del	XP_011544249.1:p.Pro658GlnfsTer4
XM_011545948.2:c.1080del	XP_011544250.1:p.Pro361GlnfsTer4
XM_017023671.1:c.1971del	XP_016879160.1:p.Pro658GlnfsTer4
XM_017023672.2:c.1965del	XP_016879161.1:p.Pro656GlnfsTer4
XM_017023673.2:c.1965del	XP_016879162.1:p.Pro656GlnfsTer4
NM_024675.4:c.1965del MANE Select	NP_078951.2:p.Pro656GlnfsTer4