Canonical Allele Identifier: CA494167699

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23637920A>T , CM000678.2:g.23637920A>T	GRCh38
NC_000016.9:g.23649241A>T , CM000678.1:g.23649241A>T	GRCh37
NC_000016.8:g.23556742A>T	NCBI36
NG_007406.1:g.8438T>A , LRG_308:g.8438T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024675.4:c.141T>A MANE Select	NP_078951.2:p.Ser47=
ENST00000261584.9:c.141T>A MANE Select	ENSP00000261584.4:p.Ser47=
NM_024675.3:c.141T>A , LRG_308t1:c.141T>A	NP_078951.2:p.Ser47=
ENST00000261584.8:c.141T>A	ENSP00000261584.4:p.Ser47=
ENST00000561514.1:c.147T>A	ENSP00000460666.1:p.Ser49=
ENST00000561514.2:c.-745T>A	ENSP00000460666.2:n.-745T>A
ENST00000561514.3:c.147T>A	ENSP00000460666.3:p.Ser49=
ENST00000565038.1:c.16T>A
ENST00000565038.2:c.141T>A	ENSP00000459882.2:p.Ser47=
ENST00000566069.6:c.141T>A	ENSP00000459237.2:p.Ser47=
ENST00000567003.1:n.419T>A
ENST00000568219.5:c.-745T>A	ENSP00000454703.2:n.-745T>A
ENST00000697374.1:c.-745T>A	ENSP00000513284.1:n.-745T>A
ENST00000697375.1:n.1488T>A
ENST00000697376.1:c.-745T>A	ENSP00000513285.1:n.-745T>A
ENST00000697377.1:c.-745T>A	ENSP00000513286.1:n.-745T>A
ENST00000697377.2:c.147T>A	ENSP00000513286.2:p.Ser49=
ENST00000697378.1:n.661T>A
ENST00000697379.1:c.-745T>A	ENSP00000513287.1:n.-745T>A
ENST00000697379.2:c.147T>A	ENSP00000513287.2:p.Ser49=
ENST00000697382.1:c.-745T>A	ENSP00000513288.1:n.-745T>A
ENST00000697383.1:c.48+3190T>A	ENSP00000513289.1:n.48+3190T>A
ENST00000697384.1:n.295T>A
XM_011545946.1:c.147T>A	XP_011544248.1:p.Ser49=
XM_011545946.2:c.147T>A	XP_011544248.1:p.Ser49=
XM_011545947.1:c.147T>A	XP_011544249.1:p.Ser49=
XM_011545947.2:c.147T>A	XP_011544249.1:p.Ser49=
XM_011545948.1:c.-745T>A	XP_011544250.1:n.-745T>A
XM_011545948.2:c.-745T>A	XP_011544250.1:n.-745T>A
XM_017023671.1:c.147T>A	XP_016879160.1:p.Ser49=
XM_017023672.2:c.141T>A	XP_016879161.1:p.Ser47=
XM_017023673.2:c.141T>A	XP_016879162.1:p.Ser47=
XR_950851.1:n.937T>A