Canonical Allele Identifier: CA2213421116

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23629271_23629273delinsTCA , CM000678.2:g.23629271_23629273delinsTCA	GRCh38
NC_000016.9:g.23640592_23640594delinsTCA , CM000678.1:g.23640592_23640594delinsTCA	GRCh37
NC_000016.8:g.23548093_23548095delinsTCA	NCBI36
NG_007406.1:g.17085_17087delinsTGA , LRG_308:g.17085_17087delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2523_2525delinsTGA	ENSP00000460666.3:p.Thr841=
ENST00000565038.2:c.214_216delinsTGA	ENSP00000459882.2:p.Ter72=
ENST00000566069.6:c.2517_2519delinsTGA	ENSP00000459237.2:p.Thr839=
ENST00000697377.2:c.2523_2525delinsTGA	ENSP00000513286.2:p.Thr841=
ENST00000697379.2:c.2523_2525delinsTGA	ENSP00000513287.2:p.Thr841=
ENST00000561514.2:c.1632_1634delinsTGA	ENSP00000460666.2:p.Thr544=
ENST00000697374.1:c.1632_1634delinsTGA	ENSP00000513284.1:p.Thr544=
ENST00000697375.1:n.3864_3866delinsTGA
ENST00000697376.1:c.1632_1634delinsTGA	ENSP00000513285.1:p.Thr544=
ENST00000697377.1:c.1632_1634delinsTGA	ENSP00000513286.1:p.Thr544=
ENST00000697378.1:n.3037_3039delinsTGA
ENST00000697379.1:c.1632_1634delinsTGA	ENSP00000513287.1:p.Thr544=
ENST00000697380.1:n.1809_1811delinsTGA
ENST00000697381.1:n.1212_1214delinsTGA
ENST00000697382.1:c.1632_1634delinsTGA	ENSP00000513288.1:p.Thr544=
ENST00000697383.1:c.51_53delinsTGA	ENSP00000513289.1:p.Thr17=
ENST00000697384.1:n.2671_2673delinsTGA
ENST00000261584.9:c.2517_2519delinsTGA MANE Select	ENSP00000261584.4:p.Thr839=
ENST00000261584.8:c.2517_2519delinsTGA	ENSP00000261584.4:p.Thr839=
ENST00000565038.1:c.89_91delinsTGA
ENST00000568219.5:c.1632_1634delinsTGA	ENSP00000454703.2:p.Thr544=
NM_024675.3:c.2517_2519delinsTGA , LRG_308t1:c.2517_2519delinsTGA	NP_078951.2:p.Thr839=
XM_011545946.1:c.2523_2525delinsTGA	XP_011544248.1:p.Thr841=
XM_011545947.1:c.2523_2525delinsTGA	XP_011544249.1:p.Thr841=
XM_011545948.1:c.1632_1634delinsTGA	XP_011544250.1:p.Thr544=
XR_950851.1:n.3313_3315delinsTGA
XM_011545946.2:c.2523_2525delinsTGA	XP_011544248.1:p.Thr841=
XM_011545947.2:c.2523_2525delinsTGA	XP_011544249.1:p.Thr841=
XM_011545948.2:c.1632_1634delinsTGA	XP_011544250.1:p.Thr544=
XM_017023671.1:c.2523_2525delinsTGA	XP_016879160.1:p.Thr841=
XM_017023672.2:c.2517_2519delinsTGA	XP_016879161.1:p.Thr839=
XM_017023673.2:c.2517_2519delinsTGA	XP_016879162.1:p.Thr839=
NM_024675.4:c.2517_2519delinsTGA MANE Select	NP_078951.2:p.Thr839=