Canonical Allele Identifier: CA2213436466

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641166C= , CM000678.2:g.23641166C=	GRCh38
NC_000016.9:g.23652487C= , CM000678.1:g.23652487C=	GRCh37
NC_000016.8:g.23559988C=	NCBI36
NG_007406.1:g.5192G= , LRG_308:g.5192G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.-861G=	ENSP00000460666.3:n.-861G=
ENST00000565038.2:c.-9G=	ENSP00000459882.2:n.-9G=
ENST00000566069.6:c.-9G=	ENSP00000459237.2:n.-9G=
ENST00000697377.2:c.-248G=	ENSP00000513286.2:n.-248G=
ENST00000697379.2:c.-154G=	ENSP00000513287.2:n.-154G=
ENST00000561514.2:c.-1752G=	ENSP00000460666.2:n.-1752G=
ENST00000697374.1:c.-1343G=	ENSP00000513284.1:n.-1343G=
ENST00000697376.1:c.-1064G=	ENSP00000513285.1:n.-1064G=
ENST00000697377.1:c.-1139G=	ENSP00000513286.1:n.-1139G=
ENST00000697379.1:c.-1045G=	ENSP00000513287.1:n.-1045G=
ENST00000697382.1:c.-1803G=	ENSP00000513288.1:n.-1803G=
ENST00000697383.1:c.-9G=	ENSP00000513289.1:n.-9G=
ENST00000697384.1:n.146G=
ENST00000261584.9:c.-9G= MANE Select	ENSP00000261584.4:n.-9G=
ENST00000261584.8:c.-9G=	ENSP00000261584.4:n.-9G=
ENST00000567003.1:n.136G=
ENST00000568219.5:c.-877G=	ENSP00000454703.2:n.-877G=
NM_024675.3:c.-9G= , LRG_308t1:c.-9G=	NP_078951.2:n.-9G=
XM_011545948.1:c.-1028G=	XP_011544250.1:n.-1028G=
XM_011545946.2:c.-861G=	XP_011544248.1:n.-861G=
XM_011545947.2:c.-861G=	XP_011544249.1:n.-861G=
XM_011545948.2:c.-1028G=	XP_011544250.1:n.-1028G=
XM_017023671.1:c.-861G=	XP_016879160.1:n.-861G=
XM_017023672.2:c.-9G=	XP_016879161.1:n.-9G=
XM_017023673.2:c.-9G=	XP_016879162.1:n.-9G=
NM_024675.4:c.-9G= MANE Select	NP_078951.2:n.-9G=