Canonical Allele Identifier: CA2213412338

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23623005T= , CM000678.2:g.23623005T=	GRCh38
NC_000016.9:g.23634326T= , CM000678.1:g.23634326T=	GRCh37
NC_000016.8:g.23541827T=	NCBI36
NG_007406.1:g.23353A= , LRG_308:g.23353A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.2966A=	ENSP00000460666.3:p.Gln989=
ENST00000565038.2:c.*441A=	ENSP00000459882.2:n.*441A=
ENST00000566069.6:c.2960A=	ENSP00000459237.2:p.Gln987=
ENST00000697377.2:c.2804A=	ENSP00000513286.2:p.Gln935=
ENST00000697379.2:c.2966A=	ENSP00000513287.2:p.Gln989=
ENST00000561514.2:c.2075A=	ENSP00000460666.2:p.Gln692=
ENST00000697374.1:c.2075A=	ENSP00000513284.1:p.Gln692=
ENST00000697375.1:n.4307A=
ENST00000697376.1:c.2075A=	ENSP00000513285.1:p.Gln692=
ENST00000697377.1:c.1913A=	ENSP00000513286.1:p.Gln638=
ENST00000697378.1:n.3480A=
ENST00000697379.1:c.2075A=	ENSP00000513287.1:p.Gln692=
ENST00000697380.1:n.2252A=
ENST00000697381.1:n.1655A=
ENST00000697382.1:c.2075A=	ENSP00000513288.1:p.Gln692=
ENST00000697383.1:c.494A=	ENSP00000513289.1:p.Gln165=
ENST00000261584.9:c.2960A= MANE Select	ENSP00000261584.4:p.Gln987=
ENST00000261584.8:c.2960A=	ENSP00000261584.4:p.Gln987=
ENST00000568219.5:c.2075A=	ENSP00000454703.2:p.Gln692=
NM_024675.3:c.2960A= , LRG_308t1:c.2960A=	NP_078951.2:p.Gln987=
XM_011545946.1:c.2966A=	XP_011544248.1:p.Gln989=
XM_011545947.1:c.2966A=	XP_011544249.1:p.Gln989=
XM_011545948.1:c.2075A=	XP_011544250.1:p.Gln692=
XR_950851.1:n.3756A=
XM_011545946.2:c.2966A=	XP_011544248.1:p.Gln989=
XM_011545947.2:c.2966A=	XP_011544249.1:p.Gln989=
XM_011545948.2:c.2075A=	XP_011544250.1:p.Gln692=
XM_017023671.1:c.2966A=	XP_016879160.1:p.Gln989=
XM_017023672.2:c.2960A=	XP_016879161.1:p.Gln987=
XM_017023673.2:c.2960A=	XP_016879162.1:p.Gln987=
NM_024675.4:c.2960A= MANE Select	NP_078951.2:p.Gln987=