Canonical Allele Identifier: CA2213433464

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23637607_23637608delinsAG , CM000678.2:g.23637607_23637608delinsAG	GRCh38
NC_000016.9:g.23648928_23648929delinsAG , CM000678.1:g.23648928_23648929delinsAG	GRCh37
NC_000016.8:g.23556429_23556430delinsAG	NCBI36
NG_007406.1:g.8750_8751delinsCT , LRG_308:g.8750_8751delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.217+242_217+243delinsCT	ENSP00000460666.3:n.217+242_217+243delinsCT
ENST00000565038.2:c.211+242_211+243delinsCT	ENSP00000459882.2:n.211+242_211+243delinsCT
ENST00000566069.6:c.211+242_211+243delinsCT	ENSP00000459237.2:n.211+242_211+243delinsCT
ENST00000697377.2:c.217+242_217+243delinsCT	ENSP00000513286.2:n.217+242_217+243delinsCT
ENST00000697379.2:c.217+242_217+243delinsCT	ENSP00000513287.2:n.217+242_217+243delinsCT
ENST00000561514.2:c.-675+242_-675+243delinsCT	ENSP00000460666.2:n.-675+242_-675+243delinsCT
ENST00000697374.1:c.-675+242_-675+243delinsCT	ENSP00000513284.1:n.-675+242_-675+243delinsCT
ENST00000697375.1:n.1558+242_1558+243delinsCT
ENST00000697376.1:c.-675+242_-675+243delinsCT	ENSP00000513285.1:n.-675+242_-675+243delinsCT
ENST00000697377.1:c.-675+242_-675+243delinsCT	ENSP00000513286.1:n.-675+242_-675+243delinsCT
ENST00000697378.1:n.731+242_731+243delinsCT
ENST00000697379.1:c.-675+242_-675+243delinsCT	ENSP00000513287.1:n.-675+242_-675+243delinsCT
ENST00000697382.1:c.-675+242_-675+243delinsCT	ENSP00000513288.1:n.-675+242_-675+243delinsCT
ENST00000697383.1:c.48+3502_48+3503delinsCT	ENSP00000513289.1:n.48+3502_48+3503delinsCT
ENST00000697384.1:n.365+242_365+243delinsCT
ENST00000261584.9:c.211+242_211+243delinsCT MANE Select	ENSP00000261584.4:n.211+242_211+243delinsCT
ENST00000261584.8:c.211+242_211+243delinsCT	ENSP00000261584.4:n.211+242_211+243delinsCT
ENST00000561514.1:c.217+242_217+243delinsCT	ENSP00000460666.1:n.217+242_217+243delinsCT
ENST00000565038.1:c.86+242_86+243delinsCT
ENST00000567003.1:n.489+242_489+243delinsCT
ENST00000568219.5:c.-675+242_-675+243delinsCT	ENSP00000454703.2:n.-675+242_-675+243delinsCT
NM_024675.3:c.211+242_211+243delinsCT , LRG_308t1:c.211+242_211+243delinsCT	NP_078951.2:n.211+242_211+243delinsCT
XM_011545946.1:c.217+242_217+243delinsCT	XP_011544248.1:n.217+242_217+243delinsCT
XM_011545947.1:c.217+242_217+243delinsCT	XP_011544249.1:n.217+242_217+243delinsCT
XM_011545948.1:c.-675+242_-675+243delinsCT	XP_011544250.1:n.-675+242_-675+243delinsCT
XR_950851.1:n.1007+242_1007+243delinsCT
XM_011545946.2:c.217+242_217+243delinsCT	XP_011544248.1:n.217+242_217+243delinsCT
XM_011545947.2:c.217+242_217+243delinsCT	XP_011544249.1:n.217+242_217+243delinsCT
XM_011545948.2:c.-675+242_-675+243delinsCT	XP_011544250.1:n.-675+242_-675+243delinsCT
XM_017023671.1:c.217+242_217+243delinsCT	XP_016879160.1:n.217+242_217+243delinsCT
XM_017023672.2:c.211+242_211+243delinsCT	XP_016879161.1:n.211+242_211+243delinsCT
XM_017023673.2:c.211+242_211+243delinsCT	XP_016879162.1:n.211+242_211+243delinsCT
NM_024675.4:c.211+242_211+243delinsCT MANE Select	NP_078951.2:n.211+242_211+243delinsCT