Canonical Allele Identifier: CA2213436452

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641149C= , CM000678.2:g.23641149C=	GRCh38
NC_000016.9:g.23652470C= , CM000678.1:g.23652470C=	GRCh37
NC_000016.8:g.23559971C=	NCBI36
NG_007406.1:g.5209G= , LRG_308:g.5209G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-844G=	ENSP00000460666.3:n.-844G=
ENST00000565038.2:c.9G=	ENSP00000459882.2:p.Glu3=
ENST00000566069.6:c.9G=	ENSP00000459237.2:p.Glu3=
ENST00000697377.2:c.-231G=	ENSP00000513286.2:n.-231G=
ENST00000697379.2:c.-137G=	ENSP00000513287.2:n.-137G=
ENST00000561514.2:c.-1735G=	ENSP00000460666.2:n.-1735G=
ENST00000697374.1:c.-1326G=	ENSP00000513284.1:n.-1326G=
ENST00000697376.1:c.-1047G=	ENSP00000513285.1:n.-1047G=
ENST00000697377.1:c.-1122G=	ENSP00000513286.1:n.-1122G=
ENST00000697379.1:c.-1028G=	ENSP00000513287.1:n.-1028G=
ENST00000697382.1:c.-1786G=	ENSP00000513288.1:n.-1786G=
ENST00000697383.1:c.9G=	ENSP00000513289.1:p.Glu3=
ENST00000697384.1:n.163G=
ENST00000261584.9:c.9G= MANE Select	ENSP00000261584.4:p.Glu3=
ENST00000261584.8:c.9G=	ENSP00000261584.4:p.Glu3=
ENST00000567003.1:n.153G=
ENST00000568219.5:c.-860G=	ENSP00000454703.2:n.-860G=
NM_024675.3:c.9G= , LRG_308t1:c.9G=	NP_078951.2:p.Glu3=
XM_011545948.1:c.-1011G=	XP_011544250.1:n.-1011G=
XM_011545946.2:c.-844G=	XP_011544248.1:n.-844G=
XM_011545947.2:c.-844G=	XP_011544249.1:n.-844G=
XM_011545948.2:c.-1011G=	XP_011544250.1:n.-1011G=
XM_017023671.1:c.-844G=	XP_016879160.1:n.-844G=
XM_017023672.2:c.9G=	XP_016879161.1:p.Glu3=
XM_017023673.2:c.9G=	XP_016879162.1:p.Glu3=
NM_024675.4:c.9G= MANE Select	NP_078951.2:p.Glu3=