Canonical Allele Identifier: CA2213432571

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23614084T= , CM000678.2:g.23614084T=	GRCh38
NC_000016.9:g.23625405T= , CM000678.1:g.23625405T=	GRCh37
NC_000016.8:g.23532906T=	NCBI36
NG_007406.1:g.32274A= , LRG_308:g.32274A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3127A=	ENSP00000460666.3:p.Lys1043=
ENST00000565038.2:c.*602A=	ENSP00000459882.2:n.*602A=
ENST00000566069.6:c.3121A=	ENSP00000459237.2:p.Lys1041=
ENST00000697377.2:c.2965A=	ENSP00000513286.2:p.Lys989=
ENST00000697379.2:c.3127A=	ENSP00000513287.2:p.Lys1043=
ENST00000561514.2:c.2236A=	ENSP00000460666.2:p.Lys746=
ENST00000697374.1:c.2236A=	ENSP00000513284.1:p.Lys746=
ENST00000697375.1:n.4468A=
ENST00000697376.1:c.2236A=	ENSP00000513285.1:p.Lys746=
ENST00000697377.1:c.2074A=	ENSP00000513286.1:p.Lys692=
ENST00000697378.1:n.3641A=
ENST00000697379.1:c.2236A=	ENSP00000513287.1:p.Lys746=
ENST00000697380.1:n.2406-6072A=
ENST00000697381.1:n.1816A=
ENST00000697382.1:c.2229-6072A=	ENSP00000513288.1:n.2229-6072A=
ENST00000697383.1:c.655A=	ENSP00000513289.1:p.Lys219=
ENST00000261584.9:c.3121A= MANE Select	ENSP00000261584.4:p.Lys1041=
ENST00000261584.8:c.3121A=	ENSP00000261584.4:p.Lys1041=
ENST00000566069.5:c.36A=
ENST00000568219.5:c.2236A=	ENSP00000454703.2:p.Lys746=
NM_024675.3:c.3121A= , LRG_308t1:c.3121A=	NP_078951.2:p.Lys1041=
XM_011545946.1:c.3127A=	XP_011544248.1:p.Lys1043=
XM_011545947.1:c.3127A=	XP_011544249.1:p.Lys1043=
XM_011545948.1:c.2236A=	XP_011544250.1:p.Lys746=
XR_950851.1:n.3910-6072A=
XM_011545946.2:c.3127A=	XP_011544248.1:p.Lys1043=
XM_011545947.2:c.3127A=	XP_011544249.1:p.Lys1043=
XM_011545948.2:c.2236A=	XP_011544250.1:p.Lys746=
XM_017023671.1:c.3119+7278A=	XP_016879160.1:n.3119+7278A=
XM_017023672.2:c.3113+7278A=	XP_016879161.1:n.3113+7278A=
XM_017023673.2:c.3121A=	XP_016879162.1:p.Lys1041=
NM_024675.4:c.3121A= MANE Select	NP_078951.2:p.Lys1041=