Canonical Allele Identifier: CA2213424253

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23603468_23603469delinsGT , CM000678.2:g.23603468_23603469delinsGT	GRCh38
NC_000016.9:g.23614789_23614790delinsGT , CM000678.1:g.23614789_23614790delinsGT	GRCh37
NC_000016.8:g.23522290_23522291delinsGT	NCBI36
NG_007406.1:g.42889_42890delinsAC , LRG_308:g.42889_42890delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3557_3558delinsAC	ENSP00000460666.3:p.His1186=
ENST00000565038.2:c.*1036_*1037delinsAC	ENSP00000459882.2:n.*1036_*1037delinsAC
ENST00000566069.6:c.*186_*187delinsAC	ENSP00000459237.2:n.*186_*187delinsAC
ENST00000697377.2:c.3395_3396delinsAC	ENSP00000513286.2:p.His1132=
ENST00000697379.2:c.3557_3558delinsAC	ENSP00000513287.2:p.His1186=
ENST00000561514.2:c.2666_2667delinsAC	ENSP00000460666.2:p.His889=
ENST00000697374.1:c.2666_2667delinsAC	ENSP00000513284.1:p.His889=
ENST00000697375.1:n.4898_4899delinsAC
ENST00000697376.1:c.*186_*187delinsAC	ENSP00000513285.1:n.*186_*187delinsAC
ENST00000697377.1:c.2504_2505delinsAC	ENSP00000513286.1:p.His835=
ENST00000697378.1:n.4071_4072delinsAC
ENST00000697379.1:c.2666_2667delinsAC	ENSP00000513287.1:p.His889=
ENST00000697380.1:n.2755_2756delinsAC
ENST00000697381.1:n.2246_2247delinsAC
ENST00000697382.1:c.*328_*329delinsAC	ENSP00000513288.1:n.*328_*329delinsAC
ENST00000697383.1:c.1085_1086delinsAC	ENSP00000513289.1:p.His362=
ENST00000261584.9:c.3551_3552delinsAC MANE Select	ENSP00000261584.4:p.His1184=
ENST00000261584.8:c.3551_3552delinsAC	ENSP00000261584.4:p.His1184=
ENST00000566069.5:c.317_318delinsAC
ENST00000568219.5:c.2666_2667delinsAC	ENSP00000454703.2:p.His889=
NM_024675.3:c.3551_3552delinsAC , LRG_308t1:c.3551_3552delinsAC	NP_078951.2:p.His1184=
XM_011545946.1:c.3557_3558delinsAC	XP_011544248.1:p.His1186=
XM_011545947.1:c.*186_*187delinsAC	XP_011544249.1:n.*186_*187delinsAC
XM_011545948.1:c.2666_2667delinsAC	XP_011544250.1:p.His889=
XR_950851.1:n.4259_4260delinsAC
XM_011545946.2:c.3557_3558delinsAC	XP_011544248.1:p.His1186=
XM_011545947.2:c.*186_*187delinsAC	XP_011544249.1:n.*186_*187delinsAC
XM_011545948.2:c.2666_2667delinsAC	XP_011544250.1:p.His889=
XM_017023671.1:c.3320_3321delinsAC	XP_016879160.1:p.His1107=
XM_017023672.2:c.3314_3315delinsAC	XP_016879161.1:p.His1105=
XM_017023673.2:c.*186_*187delinsAC	XP_016879162.1:n.*186_*187delinsAC
NM_024675.4:c.3551_3552delinsAC MANE Select	NP_078951.2:p.His1184=