Canonical Allele Identifier: CA2213428747

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635231_23635232delinsCT , CM000678.2:g.23635231_23635232delinsCT	GRCh38
NC_000016.9:g.23646552_23646553delinsCT , CM000678.1:g.23646552_23646553delinsCT	GRCh37
NC_000016.8:g.23554053_23554054delinsCT	NCBI36
NG_007406.1:g.11126_11127delinsAG , LRG_308:g.11126_11127delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1320_1321delinsAG	ENSP00000460666.3:p.Lys440=
ENST00000565038.2:c.211+2618_211+2619delinsAG	ENSP00000459882.2:n.211+2618_211+2619delinsAG
ENST00000566069.6:c.1314_1315delinsAG	ENSP00000459237.2:p.Lys438=
ENST00000697377.2:c.1320_1321delinsAG	ENSP00000513286.2:p.Lys440=
ENST00000697379.2:c.1320_1321delinsAG	ENSP00000513287.2:p.Lys440=
ENST00000561514.2:c.429_430delinsAG	ENSP00000460666.2:p.Lys143=
ENST00000697374.1:c.429_430delinsAG	ENSP00000513284.1:p.Lys143=
ENST00000697375.1:n.2661_2662delinsAG
ENST00000697376.1:c.429_430delinsAG	ENSP00000513285.1:p.Lys143=
ENST00000697377.1:c.429_430delinsAG	ENSP00000513286.1:p.Lys143=
ENST00000697378.1:n.1834_1835delinsAG
ENST00000697379.1:c.429_430delinsAG	ENSP00000513287.1:p.Lys143=
ENST00000697382.1:c.429_430delinsAG	ENSP00000513288.1:p.Lys143=
ENST00000697383.1:c.48+5878_48+5879delinsAG	ENSP00000513289.1:n.48+5878_48+5879delinsAG
ENST00000697384.1:n.1468_1469delinsAG
ENST00000261584.9:c.1314_1315delinsAG MANE Select	ENSP00000261584.4:p.Lys438=
ENST00000261584.8:c.1314_1315delinsAG	ENSP00000261584.4:p.Lys438=
ENST00000565038.1:c.86+2618_86+2619delinsAG
ENST00000568219.5:c.429_430delinsAG	ENSP00000454703.2:p.Lys143=
NM_024675.3:c.1314_1315delinsAG , LRG_308t1:c.1314_1315delinsAG	NP_078951.2:p.Lys438=
XM_011545946.1:c.1320_1321delinsAG	XP_011544248.1:p.Lys440=
XM_011545947.1:c.1320_1321delinsAG	XP_011544249.1:p.Lys440=
XM_011545948.1:c.429_430delinsAG	XP_011544250.1:p.Lys143=
XR_950851.1:n.2110_2111delinsAG
XM_011545946.2:c.1320_1321delinsAG	XP_011544248.1:p.Lys440=
XM_011545947.2:c.1320_1321delinsAG	XP_011544249.1:p.Lys440=
XM_011545948.2:c.429_430delinsAG	XP_011544250.1:p.Lys143=
XM_017023671.1:c.1320_1321delinsAG	XP_016879160.1:p.Lys440=
XM_017023672.2:c.1314_1315delinsAG	XP_016879161.1:p.Lys438=
XM_017023673.2:c.1314_1315delinsAG	XP_016879162.1:p.Lys438=
NM_024675.4:c.1314_1315delinsAG MANE Select	NP_078951.2:p.Lys438=