Canonical Allele Identifier: CA2213422180

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23629757_23629764delinsGGTAGGTT , CM000678.2:g.23629757_23629764delinsGGTAGGTT	GRCh38
NC_000016.9:g.23641078_23641085delinsGGTAGGTT , CM000678.1:g.23641078_23641085delinsGGTAGGTT	GRCh37
NC_000016.8:g.23548579_23548586delinsGGTAGGTT	NCBI36
NG_007406.1:g.16594_16601delinsAACCTACC , LRG_308:g.16594_16601delinsAACCTACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2396_2403delinsAACCTACC	ENSP00000460666.3:p.Gln799=
ENST00000565038.2:c.212-489_212-482delinsAACCTACC	ENSP00000459882.2:n.212-489_212-482delinsAACCTACC
ENST00000566069.6:c.2390_2397delinsAACCTACC	ENSP00000459237.2:p.Gln797=
ENST00000697377.2:c.2396_2403delinsAACCTACC	ENSP00000513286.2:p.Gln799=
ENST00000697379.2:c.2396_2403delinsAACCTACC	ENSP00000513287.2:p.Gln799=
ENST00000561514.2:c.1505_1512delinsAACCTACC	ENSP00000460666.2:p.Gln502=
ENST00000697374.1:c.1505_1512delinsAACCTACC	ENSP00000513284.1:p.Gln502=
ENST00000697375.1:n.3737_3744delinsAACCTACC
ENST00000697376.1:c.1505_1512delinsAACCTACC	ENSP00000513285.1:p.Gln502=
ENST00000697377.1:c.1505_1512delinsAACCTACC	ENSP00000513286.1:p.Gln502=
ENST00000697378.1:n.2910_2917delinsAACCTACC
ENST00000697379.1:c.1505_1512delinsAACCTACC	ENSP00000513287.1:p.Gln502=
ENST00000697380.1:n.1318_1325delinsAACCTACC
ENST00000697381.1:n.1085_1092delinsAACCTACC
ENST00000697382.1:c.1505_1512delinsAACCTACC	ENSP00000513288.1:p.Gln502=
ENST00000697383.1:c.49-489_49-482delinsAACCTACC	ENSP00000513289.1:n.49-489_49-482delinsAACCTACC
ENST00000697384.1:n.2544_2551delinsAACCTACC
ENST00000261584.9:c.2390_2397delinsAACCTACC MANE Select	ENSP00000261584.4:p.Gln797=
ENST00000261584.8:c.2390_2397delinsAACCTACC	ENSP00000261584.4:p.Gln797=
ENST00000565038.1:c.87-489_87-482delinsAACCTACC
ENST00000568219.5:c.1505_1512delinsAACCTACC	ENSP00000454703.2:p.Gln502=
NM_024675.3:c.2390_2397delinsAACCTACC , LRG_308t1:c.2390_2397delinsAACCTACC	NP_078951.2:p.Gln797=
XM_011545946.1:c.2396_2403delinsAACCTACC	XP_011544248.1:p.Gln799=
XM_011545947.1:c.2396_2403delinsAACCTACC	XP_011544249.1:p.Gln799=
XM_011545948.1:c.1505_1512delinsAACCTACC	XP_011544250.1:p.Gln502=
XR_950851.1:n.3186_3193delinsAACCTACC
XM_011545946.2:c.2396_2403delinsAACCTACC	XP_011544248.1:p.Gln799=
XM_011545947.2:c.2396_2403delinsAACCTACC	XP_011544249.1:p.Gln799=
XM_011545948.2:c.1505_1512delinsAACCTACC	XP_011544250.1:p.Gln502=
XM_017023671.1:c.2396_2403delinsAACCTACC	XP_016879160.1:p.Gln799=
XM_017023672.2:c.2390_2397delinsAACCTACC	XP_016879161.1:p.Gln797=
XM_017023673.2:c.2390_2397delinsAACCTACC	XP_016879162.1:p.Gln797=
NM_024675.4:c.2390_2397delinsAACCTACC MANE Select	NP_078951.2:p.Gln797=