Canonical Allele Identifier: CA2213436468

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641168A= , CM000678.2:g.23641168A=	GRCh38
NC_000016.9:g.23652489A= , CM000678.1:g.23652489A=	GRCh37
NC_000016.8:g.23559990A=	NCBI36
NG_007406.1:g.5190T= , LRG_308:g.5190T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-863T=	ENSP00000460666.3:n.-863T=
ENST00000565038.2:c.-11T=	ENSP00000459882.2:n.-11T=
ENST00000566069.6:c.-11T=	ENSP00000459237.2:n.-11T=
ENST00000697377.2:c.-250T=	ENSP00000513286.2:n.-250T=
ENST00000697379.2:c.-156T=	ENSP00000513287.2:n.-156T=
ENST00000561514.2:c.-1754T=	ENSP00000460666.2:n.-1754T=
ENST00000697374.1:c.-1345T=	ENSP00000513284.1:n.-1345T=
ENST00000697376.1:c.-1066T=	ENSP00000513285.1:n.-1066T=
ENST00000697377.1:c.-1141T=	ENSP00000513286.1:n.-1141T=
ENST00000697379.1:c.-1047T=	ENSP00000513287.1:n.-1047T=
ENST00000697382.1:c.-1805T=	ENSP00000513288.1:n.-1805T=
ENST00000697383.1:c.-11T=	ENSP00000513289.1:n.-11T=
ENST00000697384.1:n.144T=
ENST00000261584.9:c.-11T= MANE Select	ENSP00000261584.4:n.-11T=
ENST00000261584.8:c.-11T=	ENSP00000261584.4:n.-11T=
ENST00000567003.1:n.134T=
ENST00000568219.5:c.-879T=	ENSP00000454703.2:n.-879T=
NM_024675.3:c.-11T= , LRG_308t1:c.-11T=	NP_078951.2:n.-11T=
XM_011545948.1:c.-1030T=	XP_011544250.1:n.-1030T=
XM_011545946.2:c.-863T=	XP_011544248.1:n.-863T=
XM_011545947.2:c.-863T=	XP_011544249.1:n.-863T=
XM_011545948.2:c.-1030T=	XP_011544250.1:n.-1030T=
XM_017023671.1:c.-863T=	XP_016879160.1:n.-863T=
XM_017023672.2:c.-11T=	XP_016879161.1:n.-11T=
XM_017023673.2:c.-11T=	XP_016879162.1:n.-11T=
NM_024675.4:c.-11T= MANE Select	NP_078951.2:n.-11T=