Canonical Allele Identifier: CA2213436464

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641162C= , CM000678.2:g.23641162C=	GRCh38
NC_000016.9:g.23652483C= , CM000678.1:g.23652483C=	GRCh37
NC_000016.8:g.23559984C=	NCBI36
NG_007406.1:g.5196G= , LRG_308:g.5196G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-857G=	ENSP00000460666.3:n.-857G=
ENST00000565038.2:c.-5G=	ENSP00000459882.2:n.-5G=
ENST00000566069.6:c.-5G=	ENSP00000459237.2:n.-5G=
ENST00000697377.2:c.-244G=	ENSP00000513286.2:n.-244G=
ENST00000697379.2:c.-150G=	ENSP00000513287.2:n.-150G=
ENST00000561514.2:c.-1748G=	ENSP00000460666.2:n.-1748G=
ENST00000697374.1:c.-1339G=	ENSP00000513284.1:n.-1339G=
ENST00000697376.1:c.-1060G=	ENSP00000513285.1:n.-1060G=
ENST00000697377.1:c.-1135G=	ENSP00000513286.1:n.-1135G=
ENST00000697379.1:c.-1041G=	ENSP00000513287.1:n.-1041G=
ENST00000697382.1:c.-1799G=	ENSP00000513288.1:n.-1799G=
ENST00000697383.1:c.-5G=	ENSP00000513289.1:n.-5G=
ENST00000697384.1:n.150G=
ENST00000261584.9:c.-5G= MANE Select	ENSP00000261584.4:n.-5G=
ENST00000261584.8:c.-5G=	ENSP00000261584.4:n.-5G=
ENST00000567003.1:n.140G=
ENST00000568219.5:c.-873G=	ENSP00000454703.2:n.-873G=
NM_024675.3:c.-5G= , LRG_308t1:c.-5G=	NP_078951.2:n.-5G=
XM_011545948.1:c.-1024G=	XP_011544250.1:n.-1024G=
XM_011545946.2:c.-857G=	XP_011544248.1:n.-857G=
XM_011545947.2:c.-857G=	XP_011544249.1:n.-857G=
XM_011545948.2:c.-1024G=	XP_011544250.1:n.-1024G=
XM_017023671.1:c.-857G=	XP_016879160.1:n.-857G=
XM_017023672.2:c.-5G=	XP_016879161.1:n.-5G=
XM_017023673.2:c.-5G=	XP_016879162.1:n.-5G=
NM_024675.4:c.-5G= MANE Select	NP_078951.2:n.-5G=