Canonical Allele Identifier: CA2213436453

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641151C= , CM000678.2:g.23641151C=	GRCh38
NC_000016.9:g.23652472C= , CM000678.1:g.23652472C=	GRCh37
NC_000016.8:g.23559973C=	NCBI36
NG_007406.1:g.5207G= , LRG_308:g.5207G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-846G=	ENSP00000460666.3:n.-846G=
ENST00000565038.2:c.7G=	ENSP00000459882.2:p.Glu3=
ENST00000566069.6:c.7G=	ENSP00000459237.2:p.Glu3=
ENST00000697377.2:c.-233G=	ENSP00000513286.2:n.-233G=
ENST00000697379.2:c.-139G=	ENSP00000513287.2:n.-139G=
ENST00000561514.2:c.-1737G=	ENSP00000460666.2:n.-1737G=
ENST00000697374.1:c.-1328G=	ENSP00000513284.1:n.-1328G=
ENST00000697376.1:c.-1049G=	ENSP00000513285.1:n.-1049G=
ENST00000697377.1:c.-1124G=	ENSP00000513286.1:n.-1124G=
ENST00000697379.1:c.-1030G=	ENSP00000513287.1:n.-1030G=
ENST00000697382.1:c.-1788G=	ENSP00000513288.1:n.-1788G=
ENST00000697383.1:c.7G=	ENSP00000513289.1:p.Glu3=
ENST00000697384.1:n.161G=
ENST00000261584.9:c.7G= MANE Select	ENSP00000261584.4:p.Glu3=
ENST00000261584.8:c.7G=	ENSP00000261584.4:p.Glu3=
ENST00000567003.1:n.151G=
ENST00000568219.5:c.-862G=	ENSP00000454703.2:n.-862G=
NM_024675.3:c.7G= , LRG_308t1:c.7G=	NP_078951.2:p.Glu3=
XM_011545948.1:c.-1013G=	XP_011544250.1:n.-1013G=
XM_011545946.2:c.-846G=	XP_011544248.1:n.-846G=
XM_011545947.2:c.-846G=	XP_011544249.1:n.-846G=
XM_011545948.2:c.-1013G=	XP_011544250.1:n.-1013G=
XM_017023671.1:c.-846G=	XP_016879160.1:n.-846G=
XM_017023672.2:c.7G=	XP_016879161.1:p.Glu3=
XM_017023673.2:c.7G=	XP_016879162.1:p.Glu3=
NM_024675.4:c.7G= MANE Select	NP_078951.2:p.Glu3=