Canonical Allele Identifier: CA2213436467

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641167G= , CM000678.2:g.23641167G=	GRCh38
NC_000016.9:g.23652488G= , CM000678.1:g.23652488G=	GRCh37
NC_000016.8:g.23559989G=	NCBI36
NG_007406.1:g.5191C= , LRG_308:g.5191C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-862C=	ENSP00000460666.3:n.-862C=
ENST00000565038.2:c.-10C=	ENSP00000459882.2:n.-10C=
ENST00000566069.6:c.-10C=	ENSP00000459237.2:n.-10C=
ENST00000697377.2:c.-249C=	ENSP00000513286.2:n.-249C=
ENST00000697379.2:c.-155C=	ENSP00000513287.2:n.-155C=
ENST00000561514.2:c.-1753C=	ENSP00000460666.2:n.-1753C=
ENST00000697374.1:c.-1344C=	ENSP00000513284.1:n.-1344C=
ENST00000697376.1:c.-1065C=	ENSP00000513285.1:n.-1065C=
ENST00000697377.1:c.-1140C=	ENSP00000513286.1:n.-1140C=
ENST00000697379.1:c.-1046C=	ENSP00000513287.1:n.-1046C=
ENST00000697382.1:c.-1804C=	ENSP00000513288.1:n.-1804C=
ENST00000697383.1:c.-10C=	ENSP00000513289.1:n.-10C=
ENST00000697384.1:n.145C=
ENST00000261584.9:c.-10C= MANE Select	ENSP00000261584.4:n.-10C=
ENST00000261584.8:c.-10C=	ENSP00000261584.4:n.-10C=
ENST00000567003.1:n.135C=
ENST00000568219.5:c.-878C=	ENSP00000454703.2:n.-878C=
NM_024675.3:c.-10C= , LRG_308t1:c.-10C=	NP_078951.2:n.-10C=
XM_011545948.1:c.-1029C=	XP_011544250.1:n.-1029C=
XM_011545946.2:c.-862C=	XP_011544248.1:n.-862C=
XM_011545947.2:c.-862C=	XP_011544249.1:n.-862C=
XM_011545948.2:c.-1029C=	XP_011544250.1:n.-1029C=
XM_017023671.1:c.-862C=	XP_016879160.1:n.-862C=
XM_017023672.2:c.-10C=	XP_016879161.1:n.-10C=
XM_017023673.2:c.-10C=	XP_016879162.1:n.-10C=
NM_024675.4:c.-10C= MANE Select	NP_078951.2:n.-10C=