Canonical Allele Identifier: CA395130420

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23634931C>T , CM000678.2:g.23634931C>T	GRCh38
NC_000016.9:g.23646252C>T , CM000678.1:g.23646252C>T	GRCh37
NC_000016.8:g.23553753C>T	NCBI36
NG_007406.1:g.11427G>A , LRG_308:g.11427G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024675.4:c.1615G>A MANE Select	NP_078951.2:p.Val539Ile
ENST00000261584.9:c.1615G>A MANE Select	ENSP00000261584.4:p.Val539Ile
NM_024675.3:c.1615G>A , LRG_308t1:c.1615G>A	NP_078951.2:p.Val539Ile
ENST00000261584.8:c.1615G>A	ENSP00000261584.4:p.Val539Ile
ENST00000561514.2:c.730G>A	ENSP00000460666.2:p.Val244Ile
ENST00000561514.3:c.1621G>A	ENSP00000460666.3:p.Val541Ile
ENST00000565038.1:c.86+2919G>A
ENST00000565038.2:c.211+2919G>A	ENSP00000459882.2:n.211+2919G>A
ENST00000566069.6:c.1615G>A	ENSP00000459237.2:p.Val539Ile
ENST00000568219.5:c.730G>A	ENSP00000454703.2:p.Val244Ile
ENST00000697374.1:c.730G>A	ENSP00000513284.1:p.Val244Ile
ENST00000697375.1:n.2962G>A
ENST00000697376.1:c.730G>A	ENSP00000513285.1:p.Val244Ile
ENST00000697377.1:c.730G>A	ENSP00000513286.1:p.Val244Ile
ENST00000697377.2:c.1621G>A	ENSP00000513286.2:p.Val541Ile
ENST00000697378.1:n.2135G>A
ENST00000697379.1:c.730G>A	ENSP00000513287.1:p.Val244Ile
ENST00000697379.2:c.1621G>A	ENSP00000513287.2:p.Val541Ile
ENST00000697382.1:c.730G>A	ENSP00000513288.1:p.Val244Ile
ENST00000697383.1:c.49-5656G>A	ENSP00000513289.1:n.49-5656G>A
ENST00000697384.1:n.1769G>A
XM_011545946.1:c.1621G>A	XP_011544248.1:p.Val541Ile
XM_011545946.2:c.1621G>A	XP_011544248.1:p.Val541Ile
XM_011545947.1:c.1621G>A	XP_011544249.1:p.Val541Ile
XM_011545947.2:c.1621G>A	XP_011544249.1:p.Val541Ile
XM_011545948.1:c.730G>A	XP_011544250.1:p.Val244Ile
XM_011545948.2:c.730G>A	XP_011544250.1:p.Val244Ile
XM_017023671.1:c.1621G>A	XP_016879160.1:p.Val541Ile
XM_017023672.2:c.1615G>A	XP_016879161.1:p.Val539Ile
XM_017023673.2:c.1615G>A	XP_016879162.1:p.Val539Ile
XR_950851.1:n.2411G>A