Canonical Allele Identifier: CA2695197586

Gene: PALB2

Linked Data

• ClinVar Variation Id: 2673835
• ClinVar RCV Id: RCV003450452

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23607912_23608049del , CM000678.2:g.23607912_23608049del	GRCh38
NC_000016.9:g.23619233_23619370del , CM000678.1:g.23619233_23619370del	GRCh37
NC_000016.8:g.23526734_23526871del	NCBI36
NG_007406.1:g.38312_38449del , LRG_308:g.38312_38449del

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3208-34_3311del
ENST00000565038.2:c.*683-34_*786del
ENST00000566069.6:c.3202-4377_3202-4240del	ENSP00000459237.2:n.3202-4377_3202-4240de...
ENST00000697377.2:c.3046-34_3149del
ENST00000697379.2:c.3208-34_3311del
ENST00000561514.2:c.2317-34_2420del
ENST00000697374.1:c.2317-34_2420del
ENST00000697375.1:n.4549-34_4652del
ENST00000697376.1:c.2317-4377_2317-4240del	ENSP00000513285.1:n.2317-4377_2317-4240de...
ENST00000697377.1:c.2155-34_2258del
ENST00000697378.1:n.3722-34_3825del
ENST00000697379.1:c.2317-34_2420del
ENST00000697380.1:n.2406-34_2509del
ENST00000697381.1:n.1897-34_2000del
ENST00000697382.1:c.2229-34_*82del
ENST00000697383.1:c.736-34_839del
ENST00000261584.9:c.3202-34_3305del
ENST00000261584.8:c.3202-34_3305del
ENST00000566069.5:c.117-4377_117-4240del
ENST00000568219.5:c.2317-34_2420del
NM_024675.3:c.3202-34_3305del , LRG_308t1:c.3202-34_3305del
XM_011545946.1:c.3208-34_3311del
XM_011545947.1:c.3208-4377_3208-4240del	XP_011544249.1:n.3208-4377_3208-4240del
XM_011545948.1:c.2317-34_2420del
XR_950851.1:n.3910-34_4013del
XM_011545946.2:c.3208-34_3311del
XM_011545947.2:c.3208-4377_3208-4240del	XP_011544249.1:n.3208-4377_3208-4240del
XM_011545948.2:c.2317-34_2420del
XM_017023671.1:c.3120-4377_3120-4240del	XP_016879160.1:n.3120-4377_3120-4240del
XM_017023672.2:c.3114-4377_3114-4240del	XP_016879161.1:n.3114-4377_3114-4240del
XM_017023673.2:c.3202-4377_3202-4240del	XP_016879162.1:n.3202-4377_3202-4240del
NM_024675.4:c.3202-34_3305del