Canonical Allele Identifier: CA3252638964

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23614025_23614027del , CM000678.2:g.23614025_23614027del	GRCh38
NC_000016.9:g.23625346_23625348del , CM000678.1:g.23625346_23625348del	GRCh37
NC_000016.8:g.23532847_23532849del	NCBI36
NG_007406.1:g.32331_32333del , LRG_308:g.32331_32333del

Transcript Alleles

HGVS	Amino-acid Change
NM_024675.4:c.3178_3180del MANE Select	NP_078951.2:p.Cys1060del
ENST00000261584.9:c.3178_3180del MANE Select	ENSP00000261584.4:p.Cys1060del
NM_024675.3:c.3178_3180del , LRG_308t1:c.3178_3180del	NP_078951.2:p.Cys1060del
ENST00000261584.8:c.3178_3180del	ENSP00000261584.4:p.Cys1060del
ENST00000561514.2:c.2293_2295del	ENSP00000460666.2:p.Cys765del
ENST00000561514.3:c.3184_3186del	ENSP00000460666.3:p.Cys1062del
ENST00000565038.2:c.*659_*661del	ENSP00000459882.2:n.*659_*661del
ENST00000566069.5:c.93_95del
ENST00000566069.6:c.3178_3180del	ENSP00000459237.2:p.Cys1060del
ENST00000568219.5:c.2293_2295del	ENSP00000454703.2:p.Cys765del
ENST00000697374.1:c.2293_2295del	ENSP00000513284.1:p.Cys765del
ENST00000697375.1:n.4525_4527del
ENST00000697376.1:c.2293_2295del	ENSP00000513285.1:p.Cys765del
ENST00000697377.1:c.2131_2133del	ENSP00000513286.1:p.Cys711del
ENST00000697377.2:c.3022_3024del	ENSP00000513286.2:p.Cys1008del
ENST00000697378.1:n.3698_3700del
ENST00000697379.1:c.2293_2295del	ENSP00000513287.1:p.Cys765del
ENST00000697379.2:c.3184_3186del	ENSP00000513287.2:p.Cys1062del
ENST00000697380.1:n.2406-6015_2406-6013del
ENST00000697381.1:n.1873_1875del
ENST00000697382.1:c.2229-6015_2229-6013del	ENSP00000513288.1:n.2229-6015_2229-6013del
ENST00000697383.1:c.712_714del	ENSP00000513289.1:p.Cys238del
XM_011545946.1:c.3184_3186del	XP_011544248.1:p.Cys1062del
XM_011545946.2:c.3184_3186del	XP_011544248.1:p.Cys1062del
XM_011545947.1:c.3184_3186del	XP_011544249.1:p.Cys1062del
XM_011545947.2:c.3184_3186del	XP_011544249.1:p.Cys1062del
XM_011545948.1:c.2293_2295del	XP_011544250.1:p.Cys765del
XM_011545948.2:c.2293_2295del	XP_011544250.1:p.Cys765del
XM_017023671.1:c.3119+7335_3119+7337del	XP_016879160.1:n.3119+7335_3119+7337del
XM_017023672.2:c.3113+7335_3113+7337del	XP_016879161.1:n.3113+7335_3113+7337del
XM_017023673.2:c.3178_3180del	XP_016879162.1:p.Cys1060del
XR_950851.1:n.3910-6015_3910-6013del