Canonical Allele Identifier: CA2213409670

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23621366T= , CM000678.2:g.23621366T=	GRCh38
NC_000016.9:g.23632687T= , CM000678.1:g.23632687T=	GRCh37
NC_000016.8:g.23540188T=	NCBI36
NG_007406.1:g.24992A= , LRG_308:g.24992A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3115A=	ENSP00000460666.3:p.Ile1039=
ENST00000565038.2:c.*590A=	ENSP00000459882.2:n.*590A=
ENST00000566069.6:c.3109A=	ENSP00000459237.2:p.Ile1037=
ENST00000697377.2:c.2953A=	ENSP00000513286.2:p.Ile985=
ENST00000697379.2:c.3115A=	ENSP00000513287.2:p.Ile1039=
ENST00000561514.2:c.2224A=	ENSP00000460666.2:p.Ile742=
ENST00000697374.1:c.2224A=	ENSP00000513284.1:p.Ile742=
ENST00000697375.1:n.4456A=
ENST00000697376.1:c.2224A=	ENSP00000513285.1:p.Ile742=
ENST00000697377.1:c.2062A=	ENSP00000513286.1:p.Ile688=
ENST00000697378.1:n.3629A=
ENST00000697379.1:c.2224A=	ENSP00000513287.1:p.Ile742=
ENST00000697380.1:n.2401A=
ENST00000697381.1:n.1804A=
ENST00000697382.1:c.2224A=	ENSP00000513288.1:p.Ile742=
ENST00000697383.1:c.643A=	ENSP00000513289.1:p.Ile215=
ENST00000261584.9:c.3109A= MANE Select	ENSP00000261584.4:p.Ile1037=
ENST00000261584.8:c.3109A=	ENSP00000261584.4:p.Ile1037=
ENST00000566069.5:c.24A=
ENST00000568219.5:c.2224A=	ENSP00000454703.2:p.Ile742=
NM_024675.3:c.3109A= , LRG_308t1:c.3109A=	NP_078951.2:p.Ile1037=
XM_011545946.1:c.3115A=	XP_011544248.1:p.Ile1039=
XM_011545947.1:c.3115A=	XP_011544249.1:p.Ile1039=
XM_011545948.1:c.2224A=	XP_011544250.1:p.Ile742=
XR_950851.1:n.3905A=
XM_011545946.2:c.3115A=	XP_011544248.1:p.Ile1039=
XM_011545947.2:c.3115A=	XP_011544249.1:p.Ile1039=
XM_011545948.2:c.2224A=	XP_011544250.1:p.Ile742=
XM_017023671.1:c.3115A=	XP_016879160.1:p.Ile1039=
XM_017023672.2:c.3109A=	XP_016879161.1:p.Ile1037=
XM_017023673.2:c.3109A=	XP_016879162.1:p.Ile1037=
NM_024675.4:c.3109A= MANE Select	NP_078951.2:p.Ile1037=