Canonical Allele Identifier: CA2213424538

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23603628A= , CM000678.2:g.23603628A=	GRCh38
NC_000016.9:g.23614949A= , CM000678.1:g.23614949A=	GRCh37
NC_000016.8:g.23522450A=	NCBI36
NG_007406.1:g.42730T= , LRG_308:g.42730T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3398T=	ENSP00000460666.3:p.Ile1133=
ENST00000565038.2:c.*877T=	ENSP00000459882.2:n.*877T=
ENST00000566069.6:c.*27T=	ENSP00000459237.2:n.*27T=
ENST00000697377.2:c.3236T=	ENSP00000513286.2:p.Ile1079=
ENST00000697379.2:c.3398T=	ENSP00000513287.2:p.Ile1133=
ENST00000561514.2:c.2507T=	ENSP00000460666.2:p.Ile836=
ENST00000697374.1:c.2507T=	ENSP00000513284.1:p.Ile836=
ENST00000697375.1:n.4739T=
ENST00000697376.1:c.*27T=	ENSP00000513285.1:n.*27T=
ENST00000697377.1:c.2345T=	ENSP00000513286.1:p.Ile782=
ENST00000697378.1:n.3912T=
ENST00000697379.1:c.2507T=	ENSP00000513287.1:p.Ile836=
ENST00000697380.1:n.2596T=
ENST00000697381.1:n.2087T=
ENST00000697382.1:c.*169T=	ENSP00000513288.1:n.*169T=
ENST00000697383.1:c.926T=	ENSP00000513289.1:p.Ile309=
ENST00000261584.9:c.3392T= MANE Select	ENSP00000261584.4:p.Ile1131=
ENST00000261584.8:c.3392T=	ENSP00000261584.4:p.Ile1131=
ENST00000566069.5:c.158T=
ENST00000568219.5:c.2507T=	ENSP00000454703.2:p.Ile836=
NM_024675.3:c.3392T= , LRG_308t1:c.3392T=	NP_078951.2:p.Ile1131=
XM_011545946.1:c.3398T=	XP_011544248.1:p.Ile1133=
XM_011545947.1:c.*27T=	XP_011544249.1:n.*27T=
XM_011545948.1:c.2507T=	XP_011544250.1:p.Ile836=
XR_950851.1:n.4100T=
XM_011545946.2:c.3398T=	XP_011544248.1:p.Ile1133=
XM_011545947.2:c.*27T=	XP_011544249.1:n.*27T=
XM_011545948.2:c.2507T=	XP_011544250.1:p.Ile836=
XM_017023671.1:c.3161T=	XP_016879160.1:p.Ile1054=
XM_017023672.2:c.3155T=	XP_016879161.1:p.Ile1052=
XM_017023673.2:c.*27T=	XP_016879162.1:n.*27T=
NM_024675.4:c.3392T= MANE Select	NP_078951.2:p.Ile1131=