Canonical Allele Identifier: CA2213436385

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641074A= , CM000678.2:g.23641074A=	GRCh38
NC_000016.9:g.23652395A= , CM000678.1:g.23652395A=	GRCh37
NC_000016.8:g.23559896A=	NCBI36
NG_007406.1:g.5284T= , LRG_308:g.5284T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-769T=	ENSP00000460666.3:n.-769T=
ENST00000565038.2:c.48+36T=	ENSP00000459882.2:n.48+36T=
ENST00000566069.6:c.48+36T=	ENSP00000459237.2:n.48+36T=
ENST00000697377.2:c.-192+36T=	ENSP00000513286.2:n.-192+36T=
ENST00000697379.2:c.-98+36T=	ENSP00000513287.2:n.-98+36T=
ENST00000561514.2:c.-1660T=	ENSP00000460666.2:n.-1660T=
ENST00000697374.1:c.-1251T=	ENSP00000513284.1:n.-1251T=
ENST00000697376.1:c.-1008+36T=	ENSP00000513285.1:n.-1008+36T=
ENST00000697377.1:c.-1083+36T=	ENSP00000513286.1:n.-1083+36T=
ENST00000697379.1:c.-989+36T=	ENSP00000513287.1:n.-989+36T=
ENST00000697382.1:c.-1711T=	ENSP00000513288.1:n.-1711T=
ENST00000697383.1:c.48+36T=	ENSP00000513289.1:n.48+36T=
ENST00000697384.1:n.202+36T=
ENST00000261584.9:c.48+36T= MANE Select	ENSP00000261584.4:n.48+36T=
ENST00000261584.8:c.48+36T=	ENSP00000261584.4:n.48+36T=
ENST00000567003.1:n.192+36T=
ENST00000568219.5:c.-838+53T=	ENSP00000454703.2:n.-838+53T=
NM_024675.3:c.48+36T= , LRG_308t1:c.48+36T=	NP_078951.2:n.48+36T=
XM_011545946.1:c.-769T=	XP_011544248.1:n.-769T=
XM_011545947.1:c.-769T=	XP_011544249.1:n.-769T=
XM_011545948.1:c.-972+36T=	XP_011544250.1:n.-972+36T=
XR_950851.1:n.22T=
XM_011545946.2:c.-769T=	XP_011544248.1:n.-769T=
XM_011545947.2:c.-769T=	XP_011544249.1:n.-769T=
XM_011545948.2:c.-972+36T=	XP_011544250.1:n.-972+36T=
XM_017023671.1:c.-769T=	XP_016879160.1:n.-769T=
XM_017023672.2:c.48+36T=	XP_016879161.1:n.48+36T=
XM_017023673.2:c.48+36T=	XP_016879162.1:n.48+36T=
NM_024675.4:c.48+36T= MANE Select	NP_078951.2:n.48+36T=