Canonical Allele Identifier: CA3265662804

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23637861_23638089del , CM000678.2:g.23637861_23638089del	GRCh38
NC_000016.9:g.23649182_23649410del , CM000678.1:g.23649182_23649410del	GRCh37
NC_000016.8:g.23556683_23556911del	NCBI36
NG_007406.1:g.8270_8498del , LRG_308:g.8270_8498del

Transcript Alleles

HGVS	Amino-acid Change
NM_024675.3:c.90_201del , LRG_308t1:c.90_201del
NM_024675.4:c.90_201del
ENST00000261584.8:c.90_201del
ENST00000261584.9:c.90_201del
ENST00000561514.1:c.96_207del
ENST00000561514.2:c.-796_-685del
ENST00000561514.3:c.96_207del
ENST00000565038.2:c.90_201del
ENST00000566069.6:c.90_201del
ENST00000567003.1:n.368_479del
ENST00000568219.5:c.-796_-685del
ENST00000697374.1:c.-796_-685del
ENST00000697375.1:n.1437_1548del
ENST00000697376.1:c.-832_-685del
ENST00000697377.1:c.-796_-685del
ENST00000697377.2:c.96_207del
ENST00000697378.1:n.610_721del
ENST00000697379.1:c.-796_-685del
ENST00000697379.2:c.96_207del
ENST00000697382.1:c.-796_-685del
ENST00000697383.1:c.48+3022_48+3250del	ENSP00000513289.1:n.48+3022_48+3250del
ENST00000697384.1:n.244_355del
XM_011545946.1:c.96_207del
XM_011545946.2:c.96_207del
XM_011545947.1:c.96_207del
XM_011545947.2:c.96_207del
XM_011545948.1:c.-796_-685del
XM_011545948.2:c.-796_-685del
XM_017023671.1:c.96_207del
XM_017023672.2:c.90_201del
XM_017023673.2:c.90_201del
XR_950851.1:n.886_997del