Canonical Allele Identifier: CA2213436396

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641089C= , CM000678.2:g.23641089C=	GRCh38
NC_000016.9:g.23652410C= , CM000678.1:g.23652410C=	GRCh37
NC_000016.8:g.23559911C=	NCBI36
NG_007406.1:g.5269G= , LRG_308:g.5269G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-784G=	ENSP00000460666.3:n.-784G=
ENST00000565038.2:c.48+21G=	ENSP00000459882.2:n.48+21G=
ENST00000566069.6:c.48+21G=	ENSP00000459237.2:n.48+21G=
ENST00000697377.2:c.-192+21G=	ENSP00000513286.2:n.-192+21G=
ENST00000697379.2:c.-98+21G=	ENSP00000513287.2:n.-98+21G=
ENST00000561514.2:c.-1675G=	ENSP00000460666.2:n.-1675G=
ENST00000697374.1:c.-1266G=	ENSP00000513284.1:n.-1266G=
ENST00000697376.1:c.-1008+21G=	ENSP00000513285.1:n.-1008+21G=
ENST00000697377.1:c.-1083+21G=	ENSP00000513286.1:n.-1083+21G=
ENST00000697379.1:c.-989+21G=	ENSP00000513287.1:n.-989+21G=
ENST00000697382.1:c.-1726G=	ENSP00000513288.1:n.-1726G=
ENST00000697383.1:c.48+21G=	ENSP00000513289.1:n.48+21G=
ENST00000697384.1:n.202+21G=
ENST00000261584.9:c.48+21G= MANE Select	ENSP00000261584.4:n.48+21G=
ENST00000261584.8:c.48+21G=	ENSP00000261584.4:n.48+21G=
ENST00000567003.1:n.192+21G=
ENST00000568219.5:c.-838+38G=	ENSP00000454703.2:n.-838+38G=
NM_024675.3:c.48+21G= , LRG_308t1:c.48+21G=	NP_078951.2:n.48+21G=
XM_011545946.1:c.-784G=	XP_011544248.1:n.-784G=
XM_011545947.1:c.-784G=	XP_011544249.1:n.-784G=
XM_011545948.1:c.-972+21G=	XP_011544250.1:n.-972+21G=
XR_950851.1:n.7G=
XM_011545946.2:c.-784G=	XP_011544248.1:n.-784G=
XM_011545947.2:c.-784G=	XP_011544249.1:n.-784G=
XM_011545948.2:c.-972+21G=	XP_011544250.1:n.-972+21G=
XM_017023671.1:c.-784G=	XP_016879160.1:n.-784G=
XM_017023672.2:c.48+21G=	XP_016879161.1:n.48+21G=
XM_017023673.2:c.48+21G=	XP_016879162.1:n.48+21G=
NM_024675.4:c.48+21G= MANE Select	NP_078951.2:n.48+21G=