Canonical Allele Identifier: CA2213412730

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23623081_23623084delinsTCAG , CM000678.2:g.23623081_23623084delinsTCAG	GRCh38
NC_000016.9:g.23634402_23634405delinsTCAG , CM000678.1:g.23634402_23634405delinsTCAG	GRCh37
NC_000016.8:g.23541903_23541906delinsTCAG	NCBI36
NG_007406.1:g.23274_23277delinsCTGA , LRG_308:g.23274_23277delinsCTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2887_2890delinsCTGA	ENSP00000460666.3:p.Leu963=
ENST00000565038.2:c.*362_*365delinsCTGA	ENSP00000459882.2:n.*362_*365delinsCTGA
ENST00000566069.6:c.2881_2884delinsCTGA	ENSP00000459237.2:p.Leu961=
ENST00000697377.2:c.2725_2728delinsCTGA	ENSP00000513286.2:p.Leu909=
ENST00000697379.2:c.2887_2890delinsCTGA	ENSP00000513287.2:p.Leu963=
ENST00000561514.2:c.1996_1999delinsCTGA	ENSP00000460666.2:p.Leu666=
ENST00000697374.1:c.1996_1999delinsCTGA	ENSP00000513284.1:p.Leu666=
ENST00000697375.1:n.4228_4231delinsCTGA
ENST00000697376.1:c.1996_1999delinsCTGA	ENSP00000513285.1:p.Leu666=
ENST00000697377.1:c.1834_1837delinsCTGA	ENSP00000513286.1:p.Leu612=
ENST00000697378.1:n.3401_3404delinsCTGA
ENST00000697379.1:c.1996_1999delinsCTGA	ENSP00000513287.1:p.Leu666=
ENST00000697380.1:n.2173_2176delinsCTGA
ENST00000697381.1:n.1576_1579delinsCTGA
ENST00000697382.1:c.1996_1999delinsCTGA	ENSP00000513288.1:p.Leu666=
ENST00000697383.1:c.415_418delinsCTGA	ENSP00000513289.1:p.Leu139=
ENST00000261584.9:c.2881_2884delinsCTGA MANE Select	ENSP00000261584.4:p.Leu961=
ENST00000261584.8:c.2881_2884delinsCTGA	ENSP00000261584.4:p.Leu961=
ENST00000568219.5:c.1996_1999delinsCTGA	ENSP00000454703.2:p.Leu666=
NM_024675.3:c.2881_2884delinsCTGA , LRG_308t1:c.2881_2884delinsCTGA	NP_078951.2:p.Leu961=
XM_011545946.1:c.2887_2890delinsCTGA	XP_011544248.1:p.Leu963=
XM_011545947.1:c.2887_2890delinsCTGA	XP_011544249.1:p.Leu963=
XM_011545948.1:c.1996_1999delinsCTGA	XP_011544250.1:p.Leu666=
XR_950851.1:n.3677_3680delinsCTGA
XM_011545946.2:c.2887_2890delinsCTGA	XP_011544248.1:p.Leu963=
XM_011545947.2:c.2887_2890delinsCTGA	XP_011544249.1:p.Leu963=
XM_011545948.2:c.1996_1999delinsCTGA	XP_011544250.1:p.Leu666=
XM_017023671.1:c.2887_2890delinsCTGA	XP_016879160.1:p.Leu963=
XM_017023672.2:c.2881_2884delinsCTGA	XP_016879161.1:p.Leu961=
XM_017023673.2:c.2881_2884delinsCTGA	XP_016879162.1:p.Leu961=
NM_024675.4:c.2881_2884delinsCTGA MANE Select	NP_078951.2:p.Leu961=