Canonical Allele Identifier: CA2213421105

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23629268_23629269delinsGT , CM000678.2:g.23629268_23629269delinsGT	GRCh38
NC_000016.9:g.23640589_23640590delinsGT , CM000678.1:g.23640589_23640590delinsGT	GRCh37
NC_000016.8:g.23548090_23548091delinsGT	NCBI36
NG_007406.1:g.17089_17090delinsAC , LRG_308:g.17089_17090delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2527_2528delinsAC	ENSP00000460666.3:p.Thr843=
ENST00000565038.2:c.*2_*3delinsAC	ENSP00000459882.2:n.*2_*3delinsAC
ENST00000566069.6:c.2521_2522delinsAC	ENSP00000459237.2:p.Thr841=
ENST00000697377.2:c.2527_2528delinsAC	ENSP00000513286.2:p.Thr843=
ENST00000697379.2:c.2527_2528delinsAC	ENSP00000513287.2:p.Thr843=
ENST00000561514.2:c.1636_1637delinsAC	ENSP00000460666.2:p.Thr546=
ENST00000697374.1:c.1636_1637delinsAC	ENSP00000513284.1:p.Thr546=
ENST00000697375.1:n.3868_3869delinsAC
ENST00000697376.1:c.1636_1637delinsAC	ENSP00000513285.1:p.Thr546=
ENST00000697377.1:c.1636_1637delinsAC	ENSP00000513286.1:p.Thr546=
ENST00000697378.1:n.3041_3042delinsAC
ENST00000697379.1:c.1636_1637delinsAC	ENSP00000513287.1:p.Thr546=
ENST00000697380.1:n.1813_1814delinsAC
ENST00000697381.1:n.1216_1217delinsAC
ENST00000697382.1:c.1636_1637delinsAC	ENSP00000513288.1:p.Thr546=
ENST00000697383.1:c.55_56delinsAC	ENSP00000513289.1:p.Thr19=
ENST00000697384.1:n.2675_2676delinsAC
ENST00000261584.9:c.2521_2522delinsAC MANE Select	ENSP00000261584.4:p.Thr841=
ENST00000261584.8:c.2521_2522delinsAC	ENSP00000261584.4:p.Thr841=
ENST00000565038.1:c.93_94delinsAC
ENST00000568219.5:c.1636_1637delinsAC	ENSP00000454703.2:p.Thr546=
NM_024675.3:c.2521_2522delinsAC , LRG_308t1:c.2521_2522delinsAC	NP_078951.2:p.Thr841=
XM_011545946.1:c.2527_2528delinsAC	XP_011544248.1:p.Thr843=
XM_011545947.1:c.2527_2528delinsAC	XP_011544249.1:p.Thr843=
XM_011545948.1:c.1636_1637delinsAC	XP_011544250.1:p.Thr546=
XR_950851.1:n.3317_3318delinsAC
XM_011545946.2:c.2527_2528delinsAC	XP_011544248.1:p.Thr843=
XM_011545947.2:c.2527_2528delinsAC	XP_011544249.1:p.Thr843=
XM_011545948.2:c.1636_1637delinsAC	XP_011544250.1:p.Thr546=
XM_017023671.1:c.2527_2528delinsAC	XP_016879160.1:p.Thr843=
XM_017023672.2:c.2521_2522delinsAC	XP_016879161.1:p.Thr841=
XM_017023673.2:c.2521_2522delinsAC	XP_016879162.1:p.Thr841=
NM_024675.4:c.2521_2522delinsAC MANE Select	NP_078951.2:p.Thr841=