Canonical Allele Identifier: CA2695222985

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23636118_23636120delinsGG , CM000678.2:g.23636118_23636120delinsGG	GRCh38
NC_000016.9:g.23647439_23647441delinsGG , CM000678.1:g.23647439_23647441delinsGG	GRCh37
NC_000016.8:g.23554940_23554942delinsGG	NCBI36
NG_007406.1:g.10238_10240delinsCC , LRG_308:g.10238_10240delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.432_434delinsCC	ENSP00000460666.3:p.Lys144AsnfsTer?
ENST00000565038.2:c.211+1730_211+1732delinsCC	ENSP00000459882.2:n.211+1730_211+1732delinsCC
ENST00000566069.6:c.426_428delinsCC	ENSP00000459237.2:p.Lys142AsnfsTer?
ENST00000697377.2:c.432_434delinsCC	ENSP00000513286.2:p.Lys144AsnfsTer?
ENST00000697379.2:c.432_434delinsCC	ENSP00000513287.2:p.Lys144AsnfsTer?
ENST00000561514.2:c.-460_-458delinsCC	ENSP00000460666.2:n.-460_-458delinsCC
ENST00000697374.1:c.-460_-458delinsCC	ENSP00000513284.1:n.-460_-458delinsCC
ENST00000697375.1:n.1773_1775delinsCC
ENST00000697376.1:c.-460_-458delinsCC	ENSP00000513285.1:n.-460_-458delinsCC
ENST00000697377.1:c.-460_-458delinsCC	ENSP00000513286.1:n.-460_-458delinsCC
ENST00000697378.1:n.946_948delinsCC
ENST00000697379.1:c.-460_-458delinsCC	ENSP00000513287.1:n.-460_-458delinsCC
ENST00000697382.1:c.-460_-458delinsCC	ENSP00000513288.1:n.-460_-458delinsCC
ENST00000697383.1:c.48+4990_48+4992delinsCC	ENSP00000513289.1:n.48+4990_48+4992delinsCC
ENST00000697384.1:n.580_582delinsCC
ENST00000261584.9:c.426_428delinsCC MANE Select	ENSP00000261584.4:p.Lys142AsnfsTer?
ENST00000261584.8:c.426_428delinsCC	ENSP00000261584.4:p.Lys142AsnfsTer?
ENST00000565038.1:c.86+1730_86+1732delinsCC
ENST00000567003.1:n.704_706delinsCC
ENST00000568219.5:c.-460_-458delinsCC	ENSP00000454703.2:n.-460_-458delinsCC
NM_024675.3:c.426_428delinsCC , LRG_308t1:c.426_428delinsCC	NP_078951.2:p.Lys142AsnfsTer?
XM_011545946.1:c.432_434delinsCC	XP_011544248.1:p.Lys144AsnfsTer?
XM_011545947.1:c.432_434delinsCC	XP_011544249.1:p.Lys144AsnfsTer?
XM_011545948.1:c.-460_-458delinsCC	XP_011544250.1:n.-460_-458delinsCC
XR_950851.1:n.1222_1224delinsCC
XM_011545946.2:c.432_434delinsCC	XP_011544248.1:p.Lys144AsnfsTer?
XM_011545947.2:c.432_434delinsCC	XP_011544249.1:p.Lys144AsnfsTer?
XM_011545948.2:c.-460_-458delinsCC	XP_011544250.1:n.-460_-458delinsCC
XM_017023671.1:c.432_434delinsCC	XP_016879160.1:p.Lys144AsnfsTer?
XM_017023672.2:c.426_428delinsCC	XP_016879161.1:p.Lys142AsnfsTer?
XM_017023673.2:c.426_428delinsCC	XP_016879162.1:p.Lys142AsnfsTer?
NM_024675.4:c.426_428delinsCC MANE Select	NP_078951.2:p.Lys142AsnfsTer?