Canonical Allele Identifier: CA395138067

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23603560C>T , CM000678.2:g.23603560C>T	GRCh38
NC_000016.9:g.23614881C>T , CM000678.1:g.23614881C>T	GRCh37
NC_000016.8:g.23522382C>T	NCBI36
NG_007406.1:g.42798G>A , LRG_308:g.42798G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024675.4:c.3460G>A MANE Select	NP_078951.2:p.Val1154Ile
ENST00000261584.9:c.3460G>A MANE Select	ENSP00000261584.4:p.Val1154Ile
NM_024675.3:c.3460G>A , LRG_308t1:c.3460G>A	NP_078951.2:p.Val1154Ile
ENST00000261584.8:c.3460G>A	ENSP00000261584.4:p.Val1154Ile
ENST00000561514.2:c.2575G>A	ENSP00000460666.2:p.Val859Ile
ENST00000561514.3:c.3466G>A	ENSP00000460666.3:p.Val1156Ile
ENST00000565038.2:c.*945G>A	ENSP00000459882.2:n.*945G>A
ENST00000566069.5:c.226G>A
ENST00000566069.6:c.*95G>A	ENSP00000459237.2:n.*95G>A
ENST00000568219.5:c.2575G>A	ENSP00000454703.2:p.Val859Ile
ENST00000697374.1:c.2575G>A	ENSP00000513284.1:p.Val859Ile
ENST00000697375.1:n.4807G>A
ENST00000697376.1:c.*95G>A	ENSP00000513285.1:n.*95G>A
ENST00000697377.1:c.2413G>A	ENSP00000513286.1:p.Val805Ile
ENST00000697377.2:c.3304G>A	ENSP00000513286.2:p.Val1102Ile
ENST00000697378.1:n.3980G>A
ENST00000697379.1:c.2575G>A	ENSP00000513287.1:p.Val859Ile
ENST00000697379.2:c.3466G>A	ENSP00000513287.2:p.Val1156Ile
ENST00000697380.1:n.2664G>A
ENST00000697381.1:n.2155G>A
ENST00000697382.1:c.*237G>A	ENSP00000513288.1:n.*237G>A
ENST00000697383.1:c.994G>A	ENSP00000513289.1:p.Val332Ile
XM_011545946.1:c.3466G>A	XP_011544248.1:p.Val1156Ile
XM_011545946.2:c.3466G>A	XP_011544248.1:p.Val1156Ile
XM_011545947.1:c.*95G>A	XP_011544249.1:n.*95G>A
XM_011545947.2:c.*95G>A	XP_011544249.1:n.*95G>A
XM_011545948.1:c.2575G>A	XP_011544250.1:p.Val859Ile
XM_011545948.2:c.2575G>A	XP_011544250.1:p.Val859Ile
XM_017023671.1:c.3229G>A	XP_016879160.1:p.Val1077Ile
XM_017023672.2:c.3223G>A	XP_016879161.1:p.Val1075Ile
XM_017023673.2:c.*95G>A	XP_016879162.1:n.*95G>A
XR_950851.1:n.4168G>A