Canonical Allele Identifier: CA2213436550

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641271G= , CM000678.2:g.23641271G=	GRCh38
NC_000016.9:g.23652592G= , CM000678.1:g.23652592G=	GRCh37
NC_000016.8:g.23560093G=	NCBI36
NG_007406.1:g.5087C= , LRG_308:g.5087C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-966C=	ENSP00000460666.3:n.-966C=
ENST00000566069.6:c.-114C=	ENSP00000459237.2:n.-114C=
ENST00000697377.2:c.-353C=	ENSP00000513286.2:n.-353C=
ENST00000697379.2:c.-259C=	ENSP00000513287.2:n.-259C=
ENST00000561514.2:c.-1857C=	ENSP00000460666.2:n.-1857C=
ENST00000697376.1:c.-1169C=	ENSP00000513285.1:n.-1169C=
ENST00000697377.1:c.-1244C=	ENSP00000513286.1:n.-1244C=
ENST00000697379.1:c.-1150C=	ENSP00000513287.1:n.-1150C=
ENST00000697382.1:c.-1908C=	ENSP00000513288.1:n.-1908C=
ENST00000697383.1:c.-114C=	ENSP00000513289.1:n.-114C=
ENST00000697384.1:n.41C=
ENST00000261584.9:c.-114C= MANE Select	ENSP00000261584.4:n.-114C=
ENST00000261584.8:c.-114C=	ENSP00000261584.4:n.-114C=
ENST00000567003.1:n.31C=
ENST00000568219.5:c.-982C=	ENSP00000454703.2:n.-982C=
NM_024675.3:c.-114C= , LRG_308t1:c.-114C=	NP_078951.2:n.-114C=
XM_011545948.1:c.-1133C=	XP_011544250.1:n.-1133C=
XM_011545946.2:c.-966C=	XP_011544248.1:n.-966C=
XM_011545948.2:c.-1133C=	XP_011544250.1:n.-1133C=
XM_017023672.2:c.-114C=	XP_016879161.1:n.-114C=
XM_017023673.2:c.-114C=	XP_016879162.1:n.-114C=
NM_024675.4:c.-114C= MANE Select	NP_078951.2:n.-114C=