Canonical Allele Identifier: CA279501639

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23637700_23637701del , CM000678.2:g.23637700_23637701del	GRCh38
NC_000016.9:g.23649021_23649022del , CM000678.1:g.23649021_23649022del	GRCh37
NC_000016.8:g.23556522_23556523del	NCBI36
NG_007406.1:g.8659_8660del , LRG_308:g.8659_8660del

Transcript Alleles

HGVS	Amino-acid Change
NM_024675.4:c.211+151_211+152del MANE Select	NP_078951.2:n.211+151_211+152del
ENST00000261584.9:c.211+151_211+152del MANE Select	ENSP00000261584.4:n.211+151_211+152del
NM_024675.3:c.211+151_211+152del , LRG_308t1:c.211+151_211+152del	NP_078951.2:n.211+151_211+152del
ENST00000261584.8:c.211+151_211+152del	ENSP00000261584.4:n.211+151_211+152del
ENST00000561514.1:c.217+151_217+152del	ENSP00000460666.1:n.217+151_217+152del
ENST00000561514.2:c.-675+151_-675+152del	ENSP00000460666.2:n.-675+151_-675+152del
ENST00000561514.3:c.217+151_217+152del	ENSP00000460666.3:n.217+151_217+152del
ENST00000565038.1:c.86+151_86+152del
ENST00000565038.2:c.211+151_211+152del	ENSP00000459882.2:n.211+151_211+152del
ENST00000566069.6:c.211+151_211+152del	ENSP00000459237.2:n.211+151_211+152del
ENST00000567003.1:n.489+151_489+152del
ENST00000568219.5:c.-675+151_-675+152del	ENSP00000454703.2:n.-675+151_-675+152del
ENST00000697374.1:c.-675+151_-675+152del	ENSP00000513284.1:n.-675+151_-675+152del
ENST00000697375.1:n.1558+151_1558+152del
ENST00000697376.1:c.-675+151_-675+152del	ENSP00000513285.1:n.-675+151_-675+152del
ENST00000697377.1:c.-675+151_-675+152del	ENSP00000513286.1:n.-675+151_-675+152del
ENST00000697377.2:c.217+151_217+152del	ENSP00000513286.2:n.217+151_217+152del
ENST00000697378.1:n.731+151_731+152del
ENST00000697379.1:c.-675+151_-675+152del	ENSP00000513287.1:n.-675+151_-675+152del
ENST00000697379.2:c.217+151_217+152del	ENSP00000513287.2:n.217+151_217+152del
ENST00000697382.1:c.-675+151_-675+152del	ENSP00000513288.1:n.-675+151_-675+152del
ENST00000697383.1:c.48+3411_48+3412del	ENSP00000513289.1:n.48+3411_48+3412del
ENST00000697384.1:n.365+151_365+152del
XM_011545946.1:c.217+151_217+152del	XP_011544248.1:n.217+151_217+152del
XM_011545946.2:c.217+151_217+152del	XP_011544248.1:n.217+151_217+152del
XM_011545947.1:c.217+151_217+152del	XP_011544249.1:n.217+151_217+152del
XM_011545947.2:c.217+151_217+152del	XP_011544249.1:n.217+151_217+152del
XM_011545948.1:c.-675+151_-675+152del	XP_011544250.1:n.-675+151_-675+152del
XM_011545948.2:c.-675+151_-675+152del	XP_011544250.1:n.-675+151_-675+152del
XM_017023671.1:c.217+151_217+152del	XP_016879160.1:n.217+151_217+152del
XM_017023672.2:c.211+151_211+152del	XP_016879161.1:n.211+151_211+152del
XM_017023673.2:c.211+151_211+152del	XP_016879162.1:n.211+151_211+152del
XR_950851.1:n.1007+151_1007+152del