Canonical Allele Identifier: CA2499223402
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs2142271053

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23607864del , CM000678.2:g.23607864del GRCh38
NC_000016.9:g.23619185del , CM000678.1:g.23619185del GRCh37
NC_000016.8:g.23526686del NCBI36
NG_007406.1:g.38495del , LRG_308:g.38495del

Transcript Alleles

HGVS Amino-acid change
ENST00000561514.3:c.3356+1del
ENST00000565038.2:c.*832del ENSP00000459882.2:n.*832del
ENST00000566069.6:c.3202-4194del ENSP00000459237.2:n.3202-4194del
ENST00000697377.2:c.3194+1del
ENST00000697379.2:c.3356+1del
ENST00000561514.2:c.2465+1del
ENST00000697374.1:c.2465+1del
ENST00000697375.1:n.4697+1del
ENST00000697376.1:c.2317-4194del ENSP00000513285.1:n.2317-4194del
ENST00000697377.1:c.2303+1del
ENST00000697378.1:n.3870+1del
ENST00000697379.1:c.2465+1del
ENST00000697380.1:n.2554+1del
ENST00000697381.1:n.2045+1del
ENST00000697382.1:c.*127+1del
ENST00000697383.1:c.884+1del
ENST00000261584.9:c.3350+1del
ENST00000261584.8:c.3350+1del
ENST00000566069.5:c.117-4194del
ENST00000568219.5:c.2465+1del
NM_024675.3:c.3350+1del , LRG_308t1:c.3350+1del
XM_011545946.1:c.3356+1del
XM_011545947.1:c.3208-4194del XP_011544249.1:n.3208-4194del
XM_011545948.1:c.2465+1del
XR_950851.1:n.4058+1del
XM_011545946.2:c.3356+1del
XM_011545947.2:c.3208-4194del XP_011544249.1:n.3208-4194del
XM_011545948.2:c.2465+1del
XM_017023671.1:c.3120-4194del XP_016879160.1:n.3120-4194del
XM_017023672.2:c.3114-4194del XP_016879161.1:n.3114-4194del
XM_017023673.2:c.3202-4194del XP_016879162.1:n.3202-4194del
NM_024675.4:c.3350+1del