Canonical Allele Identifier: CA2213412858

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23623104T= , CM000678.2:g.23623104T=	GRCh38
NC_000016.9:g.23634425T= , CM000678.1:g.23634425T=	GRCh37
NC_000016.8:g.23541926T=	NCBI36
NG_007406.1:g.23254A= , LRG_308:g.23254A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2867A=	ENSP00000460666.3:p.Glu956=
ENST00000565038.2:c.*342A=	ENSP00000459882.2:n.*342A=
ENST00000566069.6:c.2861A=	ENSP00000459237.2:p.Glu954=
ENST00000697377.2:c.2705A=	ENSP00000513286.2:p.Glu902=
ENST00000697379.2:c.2867A=	ENSP00000513287.2:p.Glu956=
ENST00000561514.2:c.1976A=	ENSP00000460666.2:p.Glu659=
ENST00000697374.1:c.1976A=	ENSP00000513284.1:p.Glu659=
ENST00000697375.1:n.4208A=
ENST00000697376.1:c.1976A=	ENSP00000513285.1:p.Glu659=
ENST00000697377.1:c.1814A=	ENSP00000513286.1:p.Glu605=
ENST00000697378.1:n.3381A=
ENST00000697379.1:c.1976A=	ENSP00000513287.1:p.Glu659=
ENST00000697380.1:n.2153A=
ENST00000697381.1:n.1556A=
ENST00000697382.1:c.1976A=	ENSP00000513288.1:p.Glu659=
ENST00000697383.1:c.395A=	ENSP00000513289.1:p.Glu132=
ENST00000261584.9:c.2861A= MANE Select	ENSP00000261584.4:p.Glu954=
ENST00000261584.8:c.2861A=	ENSP00000261584.4:p.Glu954=
ENST00000568219.5:c.1976A=	ENSP00000454703.2:p.Glu659=
NM_024675.3:c.2861A= , LRG_308t1:c.2861A=	NP_078951.2:p.Glu954=
XM_011545946.1:c.2867A=	XP_011544248.1:p.Glu956=
XM_011545947.1:c.2867A=	XP_011544249.1:p.Glu956=
XM_011545948.1:c.1976A=	XP_011544250.1:p.Glu659=
XR_950851.1:n.3657A=
XM_011545946.2:c.2867A=	XP_011544248.1:p.Glu956=
XM_011545947.2:c.2867A=	XP_011544249.1:p.Glu956=
XM_011545948.2:c.1976A=	XP_011544250.1:p.Glu659=
XM_017023671.1:c.2867A=	XP_016879160.1:p.Glu956=
XM_017023672.2:c.2861A=	XP_016879161.1:p.Glu954=
XM_017023673.2:c.2861A=	XP_016879162.1:p.Glu954=
NM_024675.4:c.2861A= MANE Select	NP_078951.2:p.Glu954=