Canonical Allele Identifier: CA2213412472

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23623028_23623029delinsAC , CM000678.2:g.23623028_23623029delinsAC	GRCh38
NC_000016.9:g.23634349_23634350delinsAC , CM000678.1:g.23634349_23634350delinsAC	GRCh37
NC_000016.8:g.23541850_23541851delinsAC	NCBI36
NG_007406.1:g.23329_23330delinsGT , LRG_308:g.23329_23330delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2942_2943delinsGT	ENSP00000460666.3:p.Ser981=
ENST00000565038.2:c.*417_*418delinsGT	ENSP00000459882.2:n.*417_*418delinsGT
ENST00000566069.6:c.2936_2937delinsGT	ENSP00000459237.2:p.Ser979=
ENST00000697377.2:c.2780_2781delinsGT	ENSP00000513286.2:p.Ser927=
ENST00000697379.2:c.2942_2943delinsGT	ENSP00000513287.2:p.Ser981=
ENST00000561514.2:c.2051_2052delinsGT	ENSP00000460666.2:p.Ser684=
ENST00000697374.1:c.2051_2052delinsGT	ENSP00000513284.1:p.Ser684=
ENST00000697375.1:n.4283_4284delinsGT
ENST00000697376.1:c.2051_2052delinsGT	ENSP00000513285.1:p.Ser684=
ENST00000697377.1:c.1889_1890delinsGT	ENSP00000513286.1:p.Ser630=
ENST00000697378.1:n.3456_3457delinsGT
ENST00000697379.1:c.2051_2052delinsGT	ENSP00000513287.1:p.Ser684=
ENST00000697380.1:n.2228_2229delinsGT
ENST00000697381.1:n.1631_1632delinsGT
ENST00000697382.1:c.2051_2052delinsGT	ENSP00000513288.1:p.Ser684=
ENST00000697383.1:c.470_471delinsGT	ENSP00000513289.1:p.Ser157=
ENST00000261584.9:c.2936_2937delinsGT MANE Select	ENSP00000261584.4:p.Ser979=
ENST00000261584.8:c.2936_2937delinsGT	ENSP00000261584.4:p.Ser979=
ENST00000568219.5:c.2051_2052delinsGT	ENSP00000454703.2:p.Ser684=
NM_024675.3:c.2936_2937delinsGT , LRG_308t1:c.2936_2937delinsGT	NP_078951.2:p.Ser979=
XM_011545946.1:c.2942_2943delinsGT	XP_011544248.1:p.Ser981=
XM_011545947.1:c.2942_2943delinsGT	XP_011544249.1:p.Ser981=
XM_011545948.1:c.2051_2052delinsGT	XP_011544250.1:p.Ser684=
XR_950851.1:n.3732_3733delinsGT
XM_011545946.2:c.2942_2943delinsGT	XP_011544248.1:p.Ser981=
XM_011545947.2:c.2942_2943delinsGT	XP_011544249.1:p.Ser981=
XM_011545948.2:c.2051_2052delinsGT	XP_011544250.1:p.Ser684=
XM_017023671.1:c.2942_2943delinsGT	XP_016879160.1:p.Ser981=
XM_017023672.2:c.2936_2937delinsGT	XP_016879161.1:p.Ser979=
XM_017023673.2:c.2936_2937delinsGT	XP_016879162.1:p.Ser979=
NM_024675.4:c.2936_2937delinsGT MANE Select	NP_078951.2:p.Ser979=