Canonical Allele Identifier: CA494168009

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23638097T>C , CM000678.2:g.23638097T>C	GRCh38
NC_000016.9:g.23649418T>C , CM000678.1:g.23649418T>C	GRCh37
NC_000016.8:g.23556919T>C	NCBI36
NG_007406.1:g.8261A>G , LRG_308:g.8261A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024675.4:c.81A>G MANE Select	NP_078951.2:p.Glu27=
ENST00000261584.9:c.81A>G MANE Select	ENSP00000261584.4:p.Glu27=
NM_024675.3:c.81A>G , LRG_308t1:c.81A>G	NP_078951.2:p.Glu27=
ENST00000261584.8:c.81A>G	ENSP00000261584.4:p.Glu27=
ENST00000561514.1:c.87A>G	ENSP00000460666.1:p.Glu29=
ENST00000561514.2:c.-805A>G	ENSP00000460666.2:n.-805A>G
ENST00000561514.3:c.87A>G	ENSP00000460666.3:p.Glu29=
ENST00000565038.2:c.81A>G	ENSP00000459882.2:p.Glu27=
ENST00000566069.6:c.81A>G	ENSP00000459237.2:p.Glu27=
ENST00000567003.1:n.359A>G
ENST00000568219.5:c.-805A>G	ENSP00000454703.2:n.-805A>G
ENST00000697374.1:c.-805A>G	ENSP00000513284.1:n.-805A>G
ENST00000697375.1:n.1428A>G
ENST00000697376.1:c.-841A>G	ENSP00000513285.1:n.-841A>G
ENST00000697377.1:c.-805A>G	ENSP00000513286.1:n.-805A>G
ENST00000697377.2:c.87A>G	ENSP00000513286.2:p.Glu29=
ENST00000697378.1:n.601A>G
ENST00000697379.1:c.-805A>G	ENSP00000513287.1:n.-805A>G
ENST00000697379.2:c.87A>G	ENSP00000513287.2:p.Glu29=
ENST00000697382.1:c.-805A>G	ENSP00000513288.1:n.-805A>G
ENST00000697383.1:c.48+3013A>G	ENSP00000513289.1:n.48+3013A>G
ENST00000697384.1:n.235A>G
XM_011545946.1:c.87A>G	XP_011544248.1:p.Glu29=
XM_011545946.2:c.87A>G	XP_011544248.1:p.Glu29=
XM_011545947.1:c.87A>G	XP_011544249.1:p.Glu29=
XM_011545947.2:c.87A>G	XP_011544249.1:p.Glu29=
XM_011545948.1:c.-805A>G	XP_011544250.1:n.-805A>G
XM_011545948.2:c.-805A>G	XP_011544250.1:n.-805A>G
XM_017023671.1:c.87A>G	XP_016879160.1:p.Glu29=
XM_017023672.2:c.81A>G	XP_016879161.1:p.Glu27=
XM_017023673.2:c.81A>G	XP_016879162.1:p.Glu27=
XR_950851.1:n.877A>G