Canonical Allele Identifier: CA2213436400

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641097G= , CM000678.2:g.23641097G=	GRCh38
NC_000016.9:g.23652418G= , CM000678.1:g.23652418G=	GRCh37
NC_000016.8:g.23559919G=	NCBI36
NG_007406.1:g.5261C= , LRG_308:g.5261C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-792C=	ENSP00000460666.3:n.-792C=
ENST00000565038.2:c.48+13C=	ENSP00000459882.2:n.48+13C=
ENST00000566069.6:c.48+13C=	ENSP00000459237.2:n.48+13C=
ENST00000697377.2:c.-192+13C=	ENSP00000513286.2:n.-192+13C=
ENST00000697379.2:c.-98+13C=	ENSP00000513287.2:n.-98+13C=
ENST00000561514.2:c.-1683C=	ENSP00000460666.2:n.-1683C=
ENST00000697374.1:c.-1274C=	ENSP00000513284.1:n.-1274C=
ENST00000697376.1:c.-1008+13C=	ENSP00000513285.1:n.-1008+13C=
ENST00000697377.1:c.-1083+13C=	ENSP00000513286.1:n.-1083+13C=
ENST00000697379.1:c.-989+13C=	ENSP00000513287.1:n.-989+13C=
ENST00000697382.1:c.-1734C=	ENSP00000513288.1:n.-1734C=
ENST00000697383.1:c.48+13C=	ENSP00000513289.1:n.48+13C=
ENST00000697384.1:n.202+13C=
ENST00000261584.9:c.48+13C= MANE Select	ENSP00000261584.4:n.48+13C=
ENST00000261584.8:c.48+13C=	ENSP00000261584.4:n.48+13C=
ENST00000567003.1:n.192+13C=
ENST00000568219.5:c.-838+30C=	ENSP00000454703.2:n.-838+30C=
NM_024675.3:c.48+13C= , LRG_308t1:c.48+13C=	NP_078951.2:n.48+13C=
XM_011545948.1:c.-972+13C=	XP_011544250.1:n.-972+13C=
XM_011545946.2:c.-792C=	XP_011544248.1:n.-792C=
XM_011545947.2:c.-792C=	XP_011544249.1:n.-792C=
XM_011545948.2:c.-972+13C=	XP_011544250.1:n.-972+13C=
XM_017023671.1:c.-792C=	XP_016879160.1:n.-792C=
XM_017023672.2:c.48+13C=	XP_016879161.1:n.48+13C=
XM_017023673.2:c.48+13C=	XP_016879162.1:n.48+13C=
NM_024675.4:c.48+13C= MANE Select	NP_078951.2:n.48+13C=