Canonical Allele Identifier: CA2213430293

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635706_23635707delinsGT , CM000678.2:g.23635706_23635707delinsGT	GRCh38
NC_000016.9:g.23647027_23647028delinsGT , CM000678.1:g.23647027_23647028delinsGT	GRCh37
NC_000016.8:g.23554528_23554529delinsGT	NCBI36
NG_007406.1:g.10651_10652delinsAC , LRG_308:g.10651_10652delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.845_846delinsAC	ENSP00000460666.3:p.Asn282=
ENST00000565038.2:c.211+2143_211+2144delinsAC	ENSP00000459882.2:n.211+2143_211+2144delinsAC
ENST00000566069.6:c.839_840delinsAC	ENSP00000459237.2:p.Asn280=
ENST00000697377.2:c.845_846delinsAC	ENSP00000513286.2:p.Asn282=
ENST00000697379.2:c.845_846delinsAC	ENSP00000513287.2:p.Asn282=
ENST00000561514.2:c.-47_-46delinsAC	ENSP00000460666.2:n.-47_-46delinsAC
ENST00000697374.1:c.-47_-46delinsAC	ENSP00000513284.1:n.-47_-46delinsAC
ENST00000697375.1:n.2186_2187delinsAC
ENST00000697376.1:c.-47_-46delinsAC	ENSP00000513285.1:n.-47_-46delinsAC
ENST00000697377.1:c.-47_-46delinsAC	ENSP00000513286.1:n.-47_-46delinsAC
ENST00000697378.1:n.1359_1360delinsAC
ENST00000697379.1:c.-47_-46delinsAC	ENSP00000513287.1:n.-47_-46delinsAC
ENST00000697382.1:c.-47_-46delinsAC	ENSP00000513288.1:n.-47_-46delinsAC
ENST00000697383.1:c.48+5403_48+5404delinsAC	ENSP00000513289.1:n.48+5403_48+5404delinsAC
ENST00000697384.1:n.993_994delinsAC
ENST00000261584.9:c.839_840delinsAC MANE Select	ENSP00000261584.4:p.Asn280=
ENST00000261584.8:c.839_840delinsAC	ENSP00000261584.4:p.Asn280=
ENST00000565038.1:c.86+2143_86+2144delinsAC
ENST00000568219.5:c.-47_-46delinsAC	ENSP00000454703.2:n.-47_-46delinsAC
NM_024675.3:c.839_840delinsAC , LRG_308t1:c.839_840delinsAC	NP_078951.2:p.Asn280=
XM_011545946.1:c.845_846delinsAC	XP_011544248.1:p.Asn282=
XM_011545947.1:c.845_846delinsAC	XP_011544249.1:p.Asn282=
XM_011545948.1:c.-47_-46delinsAC	XP_011544250.1:n.-47_-46delinsAC
XR_950851.1:n.1635_1636delinsAC
XM_011545946.2:c.845_846delinsAC	XP_011544248.1:p.Asn282=
XM_011545947.2:c.845_846delinsAC	XP_011544249.1:p.Asn282=
XM_011545948.2:c.-47_-46delinsAC	XP_011544250.1:n.-47_-46delinsAC
XM_017023671.1:c.845_846delinsAC	XP_016879160.1:p.Asn282=
XM_017023672.2:c.839_840delinsAC	XP_016879161.1:p.Asn280=
XM_017023673.2:c.839_840delinsAC	XP_016879162.1:p.Asn280=
NM_024675.4:c.839_840delinsAC MANE Select	NP_078951.2:p.Asn280=