Canonical Allele Identifier: CA2213424257

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23603470G= , CM000678.2:g.23603470G=	GRCh38
NC_000016.9:g.23614791G= , CM000678.1:g.23614791G=	GRCh37
NC_000016.8:g.23522292G=	NCBI36
NG_007406.1:g.42888C= , LRG_308:g.42888C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3556C=	ENSP00000460666.3:p.His1186=
ENST00000565038.2:c.*1035C=	ENSP00000459882.2:n.*1035C=
ENST00000566069.6:c.*185C=	ENSP00000459237.2:n.*185C=
ENST00000697377.2:c.3394C=	ENSP00000513286.2:p.His1132=
ENST00000697379.2:c.3556C=	ENSP00000513287.2:p.His1186=
ENST00000561514.2:c.2665C=	ENSP00000460666.2:p.His889=
ENST00000697374.1:c.2665C=	ENSP00000513284.1:p.His889=
ENST00000697375.1:n.4897C=
ENST00000697376.1:c.*185C=	ENSP00000513285.1:n.*185C=
ENST00000697377.1:c.2503C=	ENSP00000513286.1:p.His835=
ENST00000697378.1:n.4070C=
ENST00000697379.1:c.2665C=	ENSP00000513287.1:p.His889=
ENST00000697380.1:n.2754C=
ENST00000697381.1:n.2245C=
ENST00000697382.1:c.*327C=	ENSP00000513288.1:n.*327C=
ENST00000697383.1:c.1084C=	ENSP00000513289.1:p.His362=
ENST00000261584.9:c.3550C= MANE Select	ENSP00000261584.4:p.His1184=
ENST00000261584.8:c.3550C=	ENSP00000261584.4:p.His1184=
ENST00000566069.5:c.316C=
ENST00000568219.5:c.2665C=	ENSP00000454703.2:p.His889=
NM_024675.3:c.3550C= , LRG_308t1:c.3550C=	NP_078951.2:p.His1184=
XM_011545946.1:c.3556C=	XP_011544248.1:p.His1186=
XM_011545947.1:c.*185C=	XP_011544249.1:n.*185C=
XM_011545948.1:c.2665C=	XP_011544250.1:p.His889=
XR_950851.1:n.4258C=
XM_011545946.2:c.3556C=	XP_011544248.1:p.His1186=
XM_011545947.2:c.*185C=	XP_011544249.1:n.*185C=
XM_011545948.2:c.2665C=	XP_011544250.1:p.His889=
XM_017023671.1:c.3319C=	XP_016879160.1:p.His1107=
XM_017023672.2:c.3313C=	XP_016879161.1:p.His1105=
XM_017023673.2:c.*185C=	XP_016879162.1:n.*185C=
NM_024675.4:c.3550C= MANE Select	NP_078951.2:p.His1184=