Canonical Allele Identifier: CA2213436391

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641083C= , CM000678.2:g.23641083C=	GRCh38
NC_000016.9:g.23652404C= , CM000678.1:g.23652404C=	GRCh37
NC_000016.8:g.23559905C=	NCBI36
NG_007406.1:g.5275G= , LRG_308:g.5275G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-778G=	ENSP00000460666.3:n.-778G=
ENST00000565038.2:c.48+27G=	ENSP00000459882.2:n.48+27G=
ENST00000566069.6:c.48+27G=	ENSP00000459237.2:n.48+27G=
ENST00000697377.2:c.-192+27G=	ENSP00000513286.2:n.-192+27G=
ENST00000697379.2:c.-98+27G=	ENSP00000513287.2:n.-98+27G=
ENST00000561514.2:c.-1669G=	ENSP00000460666.2:n.-1669G=
ENST00000697374.1:c.-1260G=	ENSP00000513284.1:n.-1260G=
ENST00000697376.1:c.-1008+27G=	ENSP00000513285.1:n.-1008+27G=
ENST00000697377.1:c.-1083+27G=	ENSP00000513286.1:n.-1083+27G=
ENST00000697379.1:c.-989+27G=	ENSP00000513287.1:n.-989+27G=
ENST00000697382.1:c.-1720G=	ENSP00000513288.1:n.-1720G=
ENST00000697383.1:c.48+27G=	ENSP00000513289.1:n.48+27G=
ENST00000697384.1:n.202+27G=
ENST00000261584.9:c.48+27G= MANE Select	ENSP00000261584.4:n.48+27G=
ENST00000261584.8:c.48+27G=	ENSP00000261584.4:n.48+27G=
ENST00000567003.1:n.192+27G=
ENST00000568219.5:c.-838+44G=	ENSP00000454703.2:n.-838+44G=
NM_024675.3:c.48+27G= , LRG_308t1:c.48+27G=	NP_078951.2:n.48+27G=
XM_011545946.1:c.-778G=	XP_011544248.1:n.-778G=
XM_011545947.1:c.-778G=	XP_011544249.1:n.-778G=
XM_011545948.1:c.-972+27G=	XP_011544250.1:n.-972+27G=
XR_950851.1:n.13G=
XM_011545946.2:c.-778G=	XP_011544248.1:n.-778G=
XM_011545947.2:c.-778G=	XP_011544249.1:n.-778G=
XM_011545948.2:c.-972+27G=	XP_011544250.1:n.-972+27G=
XM_017023671.1:c.-778G=	XP_016879160.1:n.-778G=
XM_017023672.2:c.48+27G=	XP_016879161.1:n.48+27G=
XM_017023673.2:c.48+27G=	XP_016879162.1:n.48+27G=
NM_024675.4:c.48+27G= MANE Select	NP_078951.2:n.48+27G=