Canonical Allele Identifier: CA2580613445
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2567556
ClinVar RCV Id: RCV003311295

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23607863_23607864delinsG , CM000678.2:g.23607863_23607864delinsG GRCh38
NC_000016.9:g.23619184_23619185delinsG , CM000678.1:g.23619184_23619185delinsG GRCh37
NC_000016.8:g.23526685_23526686delinsG NCBI36
NG_007406.1:g.38494_38495delinsC , LRG_308:g.38494_38495delinsC

Transcript Alleles

HGVS Amino-acid change
ENST00000561514.3:c.3356_3356+1delinsC
ENST00000565038.2:c.*831_*832delinsC ENSP00000459882.2:n.*831_*832delinsC
ENST00000566069.6:c.3202-4195_3202-4194delinsC ENSP00000459237.2:n.3202-4195_3202-4194de...
ENST00000697377.2:c.3194_3194+1delinsC
ENST00000697379.2:c.3356_3356+1delinsC
ENST00000561514.2:c.2465_2465+1delinsC
ENST00000697374.1:c.2465_2465+1delinsC
ENST00000697375.1:n.4697_4697+1delinsC
ENST00000697376.1:c.2317-4195_2317-4194delinsC ENSP00000513285.1:n.2317-4195_2317-4194de...
ENST00000697377.1:c.2303_2303+1delinsC
ENST00000697378.1:n.3870_3870+1delinsC
ENST00000697379.1:c.2465_2465+1delinsC
ENST00000697380.1:n.2554_2554+1delinsC
ENST00000697381.1:n.2045_2045+1delinsC
ENST00000697382.1:c.*127_*127+1delinsC
ENST00000697383.1:c.884_884+1delinsC
ENST00000261584.9:c.3350_3350+1delinsC
ENST00000261584.8:c.3350_3350+1delinsC
ENST00000566069.5:c.117-4195_117-4194delinsC
ENST00000568219.5:c.2465_2465+1delinsC
NM_024675.3:c.3350_3350+1delinsC , LRG_308t1:c.3350_3350+1delinsC
XM_011545946.1:c.3356_3356+1delinsC
XM_011545947.1:c.3208-4195_3208-4194delinsC XP_011544249.1:n.3208-4195_3208-4194delin...
XM_011545948.1:c.2465_2465+1delinsC
XR_950851.1:n.4058_4058+1delinsC
XM_011545946.2:c.3356_3356+1delinsC
XM_011545947.2:c.3208-4195_3208-4194delinsC XP_011544249.1:n.3208-4195_3208-4194delin...
XM_011545948.2:c.2465_2465+1delinsC
XM_017023671.1:c.3120-4195_3120-4194delinsC XP_016879160.1:n.3120-4195_3120-4194delin...
XM_017023672.2:c.3114-4195_3114-4194delinsC XP_016879161.1:n.3114-4195_3114-4194delin...
XM_017023673.2:c.3202-4195_3202-4194delinsC XP_016879162.1:n.3202-4195_3202-4194delin...
NM_024675.4:c.3350_3350+1delinsC