Canonical Allele Identifier: CA2213436433

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641129C= , CM000678.2:g.23641129C=	GRCh38
NC_000016.9:g.23652450C= , CM000678.1:g.23652450C=	GRCh37
NC_000016.8:g.23559951C=	NCBI36
NG_007406.1:g.5229G= , LRG_308:g.5229G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-824G=	ENSP00000460666.3:n.-824G=
ENST00000565038.2:c.29G=	ENSP00000459882.2:p.Ser10=
ENST00000566069.6:c.29G=	ENSP00000459237.2:p.Ser10=
ENST00000697377.2:c.-211G=	ENSP00000513286.2:n.-211G=
ENST00000697379.2:c.-117G=	ENSP00000513287.2:n.-117G=
ENST00000561514.2:c.-1715G=	ENSP00000460666.2:n.-1715G=
ENST00000697374.1:c.-1306G=	ENSP00000513284.1:n.-1306G=
ENST00000697376.1:c.-1027G=	ENSP00000513285.1:n.-1027G=
ENST00000697377.1:c.-1102G=	ENSP00000513286.1:n.-1102G=
ENST00000697379.1:c.-1008G=	ENSP00000513287.1:n.-1008G=
ENST00000697382.1:c.-1766G=	ENSP00000513288.1:n.-1766G=
ENST00000697383.1:c.29G=	ENSP00000513289.1:p.Ser10=
ENST00000697384.1:n.183G=
ENST00000261584.9:c.29G= MANE Select	ENSP00000261584.4:p.Ser10=
ENST00000261584.8:c.29G=	ENSP00000261584.4:p.Ser10=
ENST00000567003.1:n.173G=
ENST00000568219.5:c.-840G=	ENSP00000454703.2:n.-840G=
NM_024675.3:c.29G= , LRG_308t1:c.29G=	NP_078951.2:p.Ser10=
XM_011545948.1:c.-991G=	XP_011544250.1:n.-991G=
XM_011545946.2:c.-824G=	XP_011544248.1:n.-824G=
XM_011545947.2:c.-824G=	XP_011544249.1:n.-824G=
XM_011545948.2:c.-991G=	XP_011544250.1:n.-991G=
XM_017023671.1:c.-824G=	XP_016879160.1:n.-824G=
XM_017023672.2:c.29G=	XP_016879161.1:p.Ser10=
XM_017023673.2:c.29G=	XP_016879162.1:p.Ser10=
NM_024675.4:c.29G= MANE Select	NP_078951.2:p.Ser10=