Canonical Allele Identifier: CA2213436458

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641156A= , CM000678.2:g.23641156A=	GRCh38
NC_000016.9:g.23652477A= , CM000678.1:g.23652477A=	GRCh37
NC_000016.8:g.23559978A=	NCBI36
NG_007406.1:g.5202T= , LRG_308:g.5202T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.-851T=	ENSP00000460666.3:n.-851T=
ENST00000565038.2:c.2T=	ENSP00000459882.2:p.Met1=
ENST00000566069.6:c.2T=	ENSP00000459237.2:p.Met1=
ENST00000697377.2:c.-238T=	ENSP00000513286.2:n.-238T=
ENST00000697379.2:c.-144T=	ENSP00000513287.2:n.-144T=
ENST00000561514.2:c.-1742T=	ENSP00000460666.2:n.-1742T=
ENST00000697374.1:c.-1333T=	ENSP00000513284.1:n.-1333T=
ENST00000697376.1:c.-1054T=	ENSP00000513285.1:n.-1054T=
ENST00000697377.1:c.-1129T=	ENSP00000513286.1:n.-1129T=
ENST00000697379.1:c.-1035T=	ENSP00000513287.1:n.-1035T=
ENST00000697382.1:c.-1793T=	ENSP00000513288.1:n.-1793T=
ENST00000697383.1:c.2T=	ENSP00000513289.1:p.Met1=
ENST00000697384.1:n.156T=
ENST00000261584.9:c.2T= MANE Select	ENSP00000261584.4:p.Met1=
ENST00000261584.8:c.2T=	ENSP00000261584.4:p.Met1=
ENST00000567003.1:n.146T=
ENST00000568219.5:c.-867T=	ENSP00000454703.2:n.-867T=
NM_024675.3:c.2T= , LRG_308t1:c.2T=	NP_078951.2:p.Met1=
XM_011545948.1:c.-1018T=	XP_011544250.1:n.-1018T=
XM_011545946.2:c.-851T=	XP_011544248.1:n.-851T=
XM_011545947.2:c.-851T=	XP_011544249.1:n.-851T=
XM_011545948.2:c.-1018T=	XP_011544250.1:n.-1018T=
XM_017023671.1:c.-851T=	XP_016879160.1:n.-851T=
XM_017023672.2:c.2T=	XP_016879161.1:p.Met1=
XM_017023673.2:c.2T=	XP_016879162.1:p.Met1=
NM_024675.4:c.2T= MANE Select	NP_078951.2:p.Met1=