Canonical Allele Identifier: CA2739266663
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2799895
ClinVar RCV Id: RCV003607749

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621389_23621391del , CM000678.2:g.23621389_23621391del GRCh38
NC_000016.9:g.23632710_23632712del , CM000678.1:g.23632710_23632712del GRCh37
NC_000016.8:g.23540211_23540213del NCBI36
NG_007406.1:g.24972_24974del , LRG_308:g.24972_24974del

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3095_3097del ENSP00000460666.3:p.Thr1032del
ENST00000565038.2:c.*570_*572del ENSP00000459882.2:n.*570_*572del
ENST00000566069.6:c.3089_3091del ENSP00000459237.2:p.Thr1030del
ENST00000697377.2:c.2933_2935del ENSP00000513286.2:p.Thr978del
ENST00000697379.2:c.3095_3097del ENSP00000513287.2:p.Thr1032del
ENST00000561514.2:c.2204_2206del ENSP00000460666.2:p.Thr735del
ENST00000697374.1:c.2204_2206del ENSP00000513284.1:p.Thr735del
ENST00000697375.1:n.4436_4438del
ENST00000697376.1:c.2204_2206del ENSP00000513285.1:p.Thr735del
ENST00000697377.1:c.2042_2044del ENSP00000513286.1:p.Thr681del
ENST00000697378.1:n.3609_3611del
ENST00000697379.1:c.2204_2206del ENSP00000513287.1:p.Thr735del
ENST00000697380.1:n.2381_2383del
ENST00000697381.1:n.1784_1786del
ENST00000697382.1:c.2204_2206del ENSP00000513288.1:p.Thr735del
ENST00000697383.1:c.623_625del ENSP00000513289.1:p.Thr208del
ENST00000261584.9:c.3089_3091del MANE Select ENSP00000261584.4:p.Thr1030del
ENST00000261584.8:c.3089_3091del ENSP00000261584.4:p.Thr1030del
ENST00000568219.5:c.2204_2206del ENSP00000454703.2:p.Thr735del
NM_024675.3:c.3089_3091del , LRG_308t1:c.3089_3091del NP_078951.2:p.Thr1030del
XM_011545946.1:c.3095_3097del XP_011544248.1:p.Thr1032del
XM_011545947.1:c.3095_3097del XP_011544249.1:p.Thr1032del
XM_011545948.1:c.2204_2206del XP_011544250.1:p.Thr735del
XR_950851.1:n.3885_3887del
XM_011545946.2:c.3095_3097del XP_011544248.1:p.Thr1032del
XM_011545947.2:c.3095_3097del XP_011544249.1:p.Thr1032del
XM_011545948.2:c.2204_2206del XP_011544250.1:p.Thr735del
XM_017023671.1:c.3095_3097del XP_016879160.1:p.Thr1032del
XM_017023672.2:c.3089_3091del XP_016879161.1:p.Thr1030del
XM_017023673.2:c.3089_3091del XP_016879162.1:p.Thr1030del
NM_024675.4:c.3089_3091del MANE Select NP_078951.2:p.Thr1030del