Canonical Allele Identifier: CA2830557184

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635579_23635580insATGTT , CM000678.2:g.23635579_23635580insATGTT	GRCh38
NC_000016.9:g.23646900_23646901insATGTT , CM000678.1:g.23646900_23646901insATGTT	GRCh37
NC_000016.8:g.23554401_23554402insATGTT	NCBI36
NG_007406.1:g.10778_10779insAACAT , LRG_308:g.10778_10779insAACAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.972_973insAACAT	ENSP00000460666.3:p.Ala325AsnfsTer9
ENST00000565038.2:c.211+2270_211+2271insAACAT	ENSP00000459882.2:n.211+2270_211+2271insAACAT
ENST00000566069.6:c.966_967insAACAT	ENSP00000459237.2:p.Ala323AsnfsTer9
ENST00000697377.2:c.972_973insAACAT	ENSP00000513286.2:p.Ala325AsnfsTer9
ENST00000697379.2:c.972_973insAACAT	ENSP00000513287.2:p.Ala325AsnfsTer9
ENST00000561514.2:c.81_82insAACAT	ENSP00000460666.2:p.Ala28AsnfsTer9
ENST00000697374.1:c.81_82insAACAT	ENSP00000513284.1:p.Ala28AsnfsTer9
ENST00000697375.1:n.2313_2314insAACAT
ENST00000697376.1:c.81_82insAACAT	ENSP00000513285.1:p.Ala28AsnfsTer9
ENST00000697377.1:c.81_82insAACAT	ENSP00000513286.1:p.Ala28AsnfsTer9
ENST00000697378.1:n.1486_1487insAACAT
ENST00000697379.1:c.81_82insAACAT	ENSP00000513287.1:p.Ala28AsnfsTer9
ENST00000697382.1:c.81_82insAACAT	ENSP00000513288.1:p.Ala28AsnfsTer9
ENST00000697383.1:c.48+5530_48+5531insAACAT	ENSP00000513289.1:n.48+5530_48+5531insAACAT
ENST00000697384.1:n.1120_1121insAACAT
ENST00000261584.9:c.966_967insAACAT MANE Select	ENSP00000261584.4:p.Ala323AsnfsTer9
ENST00000261584.8:c.966_967insAACAT	ENSP00000261584.4:p.Ala323AsnfsTer9
ENST00000565038.1:c.86+2270_86+2271insAACAT
ENST00000568219.5:c.81_82insAACAT	ENSP00000454703.2:p.Ala28AsnfsTer9
NM_024675.3:c.966_967insAACAT , LRG_308t1:c.966_967insAACAT	NP_078951.2:p.Ala323AsnfsTer9
XM_011545946.1:c.972_973insAACAT	XP_011544248.1:p.Ala325AsnfsTer9
XM_011545947.1:c.972_973insAACAT	XP_011544249.1:p.Ala325AsnfsTer9
XM_011545948.1:c.81_82insAACAT	XP_011544250.1:p.Ala28AsnfsTer9
XR_950851.1:n.1762_1763insAACAT
XM_011545946.2:c.972_973insAACAT	XP_011544248.1:p.Ala325AsnfsTer9
XM_011545947.2:c.972_973insAACAT	XP_011544249.1:p.Ala325AsnfsTer9
XM_011545948.2:c.81_82insAACAT	XP_011544250.1:p.Ala28AsnfsTer9
XM_017023671.1:c.972_973insAACAT	XP_016879160.1:p.Ala325AsnfsTer9
XM_017023672.2:c.966_967insAACAT	XP_016879161.1:p.Ala323AsnfsTer9
XM_017023673.2:c.966_967insAACAT	XP_016879162.1:p.Ala323AsnfsTer9
NM_024675.4:c.966_967insAACAT MANE Select	NP_078951.2:p.Ala323AsnfsTer9