Canonical Allele Identifier: CA2213428156

Gene: PALB2

Linked Data

• dbSNP Id: rs1966965168

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635077_23635078insACTTTAGTTA , CM000678.2:g.23635077_23635078insACTTTAGTTA	GRCh38
NC_000016.9:g.23646398_23646399insACTTTAGTTA , CM000678.1:g.23646398_23646399insACTTTAGTTA	GRCh37
NC_000016.8:g.23553899_23553900insACTTTAGTTA	NCBI36
NG_007406.1:g.11280_11281insTAACTAAAGT , LRG_308:g.11280_11281insTAACTAAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1474_1475insTAACTAAAGT	ENSP00000460666.3:p.Pro492LeufsTer9
ENST00000565038.2:c.211+2772_211+2773insTAACTAAAGT	ENSP00000459882.2:n.211+2772_211+2773insTAACTAAAGT
ENST00000566069.6:c.1468_1469insTAACTAAAGT	ENSP00000459237.2:p.Pro490LeufsTer9
ENST00000697377.2:c.1474_1475insTAACTAAAGT	ENSP00000513286.2:p.Pro492LeufsTer9
ENST00000697379.2:c.1474_1475insTAACTAAAGT	ENSP00000513287.2:p.Pro492LeufsTer9
ENST00000561514.2:c.583_584insTAACTAAAGT	ENSP00000460666.2:p.Pro195LeufsTer9
ENST00000697374.1:c.583_584insTAACTAAAGT	ENSP00000513284.1:p.Pro195LeufsTer9
ENST00000697375.1:n.2815_2816insTAACTAAAGT
ENST00000697376.1:c.583_584insTAACTAAAGT	ENSP00000513285.1:p.Pro195LeufsTer9
ENST00000697377.1:c.583_584insTAACTAAAGT	ENSP00000513286.1:p.Pro195LeufsTer9
ENST00000697378.1:n.1988_1989insTAACTAAAGT
ENST00000697379.1:c.583_584insTAACTAAAGT	ENSP00000513287.1:p.Pro195LeufsTer9
ENST00000697382.1:c.583_584insTAACTAAAGT	ENSP00000513288.1:p.Pro195LeufsTer9
ENST00000697383.1:c.49-5803_49-5802insTAACTAAAGT	ENSP00000513289.1:n.49-5803_49-5802insTAACTAAAGT
ENST00000697384.1:n.1622_1623insTAACTAAAGT
ENST00000261584.9:c.1468_1469insTAACTAAAGT MANE Select	ENSP00000261584.4:p.Pro490LeufsTer9
ENST00000261584.8:c.1468_1469insTAACTAAAGT	ENSP00000261584.4:p.Pro490LeufsTer9
ENST00000565038.1:c.86+2772_86+2773insTAACTAAAGT
ENST00000568219.5:c.583_584insTAACTAAAGT	ENSP00000454703.2:p.Pro195LeufsTer9
NM_024675.3:c.1468_1469insTAACTAAAGT , LRG_308t1:c.1468_1469insTAACTAAAGT	NP_078951.2:p.Pro490LeufsTer9
XM_011545946.1:c.1474_1475insTAACTAAAGT	XP_011544248.1:p.Pro492LeufsTer9
XM_011545947.1:c.1474_1475insTAACTAAAGT	XP_011544249.1:p.Pro492LeufsTer9
XM_011545948.1:c.583_584insTAACTAAAGT	XP_011544250.1:p.Pro195LeufsTer9
XR_950851.1:n.2264_2265insTAACTAAAGT
XM_011545946.2:c.1474_1475insTAACTAAAGT	XP_011544248.1:p.Pro492LeufsTer9
XM_011545947.2:c.1474_1475insTAACTAAAGT	XP_011544249.1:p.Pro492LeufsTer9
XM_011545948.2:c.583_584insTAACTAAAGT	XP_011544250.1:p.Pro195LeufsTer9
XM_017023671.1:c.1474_1475insTAACTAAAGT	XP_016879160.1:p.Pro492LeufsTer9
XM_017023672.2:c.1468_1469insTAACTAAAGT	XP_016879161.1:p.Pro490LeufsTer9
XM_017023673.2:c.1468_1469insTAACTAAAGT	XP_016879162.1:p.Pro490LeufsTer9
NM_024675.4:c.1468_1469insTAACTAAAGT MANE Select	NP_078951.2:p.Pro490LeufsTer9