Canonical Allele Identifier: CA2213422216

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23629762_23629763delinsGT , CM000678.2:g.23629762_23629763delinsGT	GRCh38
NC_000016.9:g.23641083_23641084delinsGT , CM000678.1:g.23641083_23641084delinsGT	GRCh37
NC_000016.8:g.23548584_23548585delinsGT	NCBI36
NG_007406.1:g.16595_16596delinsAC , LRG_308:g.16595_16596delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2397_2398delinsAC	ENSP00000460666.3:p.Gln799=
ENST00000565038.2:c.212-488_212-487delinsAC	ENSP00000459882.2:n.212-488_212-487delinsAC
ENST00000566069.6:c.2391_2392delinsAC	ENSP00000459237.2:p.Gln797=
ENST00000697377.2:c.2397_2398delinsAC	ENSP00000513286.2:p.Gln799=
ENST00000697379.2:c.2397_2398delinsAC	ENSP00000513287.2:p.Gln799=
ENST00000561514.2:c.1506_1507delinsAC	ENSP00000460666.2:p.Gln502=
ENST00000697374.1:c.1506_1507delinsAC	ENSP00000513284.1:p.Gln502=
ENST00000697375.1:n.3738_3739delinsAC
ENST00000697376.1:c.1506_1507delinsAC	ENSP00000513285.1:p.Gln502=
ENST00000697377.1:c.1506_1507delinsAC	ENSP00000513286.1:p.Gln502=
ENST00000697378.1:n.2911_2912delinsAC
ENST00000697379.1:c.1506_1507delinsAC	ENSP00000513287.1:p.Gln502=
ENST00000697380.1:n.1319_1320delinsAC
ENST00000697381.1:n.1086_1087delinsAC
ENST00000697382.1:c.1506_1507delinsAC	ENSP00000513288.1:p.Gln502=
ENST00000697383.1:c.49-488_49-487delinsAC	ENSP00000513289.1:n.49-488_49-487delinsAC
ENST00000697384.1:n.2545_2546delinsAC
ENST00000261584.9:c.2391_2392delinsAC MANE Select	ENSP00000261584.4:p.Gln797=
ENST00000261584.8:c.2391_2392delinsAC	ENSP00000261584.4:p.Gln797=
ENST00000565038.1:c.87-488_87-487delinsAC
ENST00000568219.5:c.1506_1507delinsAC	ENSP00000454703.2:p.Gln502=
NM_024675.3:c.2391_2392delinsAC , LRG_308t1:c.2391_2392delinsAC	NP_078951.2:p.Gln797=
XM_011545946.1:c.2397_2398delinsAC	XP_011544248.1:p.Gln799=
XM_011545947.1:c.2397_2398delinsAC	XP_011544249.1:p.Gln799=
XM_011545948.1:c.1506_1507delinsAC	XP_011544250.1:p.Gln502=
XR_950851.1:n.3187_3188delinsAC
XM_011545946.2:c.2397_2398delinsAC	XP_011544248.1:p.Gln799=
XM_011545947.2:c.2397_2398delinsAC	XP_011544249.1:p.Gln799=
XM_011545948.2:c.1506_1507delinsAC	XP_011544250.1:p.Gln502=
XM_017023671.1:c.2397_2398delinsAC	XP_016879160.1:p.Gln799=
XM_017023672.2:c.2391_2392delinsAC	XP_016879161.1:p.Gln797=
XM_017023673.2:c.2391_2392delinsAC	XP_016879162.1:p.Gln797=
NM_024675.4:c.2391_2392delinsAC MANE Select	NP_078951.2:p.Gln797=