Canonical Allele Identifier: CA2213428662

Gene: PALB2

Linked Data

• dbSNP Id: rs1966502551

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23607723_23607760del , CM000678.2:g.23607723_23607760del	GRCh38
NC_000016.9:g.23619044_23619081del , CM000678.1:g.23619044_23619081del	GRCh37
NC_000016.8:g.23526545_23526582del	NCBI36
NG_007406.1:g.38600_38637del , LRG_308:g.38600_38637del

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3356+106_3356+143del	ENSP00000460666.3:n.3356+106_3356+143del
ENST00000565038.2:c.*835+102_*835+139del	ENSP00000459882.2:n.*835+102_*835+139del
ENST00000566069.6:c.3202-4089_3202-4052del	ENSP00000459237.2:n.3202-4089_3202-4052del
ENST00000697377.2:c.3194+106_3194+143del	ENSP00000513286.2:n.3194+106_3194+143del
ENST00000697379.2:c.3356+106_3356+143del	ENSP00000513287.2:n.3356+106_3356+143del
ENST00000561514.2:c.2465+106_2465+143del	ENSP00000460666.2:n.2465+106_2465+143del
ENST00000697374.1:c.2465+106_2465+143del	ENSP00000513284.1:n.2465+106_2465+143del
ENST00000697375.1:n.4697+106_4697+143del
ENST00000697376.1:c.2317-4089_2317-4052del	ENSP00000513285.1:n.2317-4089_2317-4052del
ENST00000697377.1:c.2303+106_2303+143del	ENSP00000513286.1:n.2303+106_2303+143del
ENST00000697378.1:n.3870+106_3870+143del
ENST00000697379.1:c.2465+106_2465+143del	ENSP00000513287.1:n.2465+106_2465+143del
ENST00000697380.1:n.2554+106_2554+143del
ENST00000697381.1:n.2045+106_2045+143del
ENST00000697382.1:c.*127+106_*127+143del	ENSP00000513288.1:n.*127+106_*127+143del
ENST00000697383.1:c.884+106_884+143del	ENSP00000513289.1:n.884+106_884+143del
ENST00000261584.9:c.3350+106_3350+143del MANE Select	ENSP00000261584.4:n.3350+106_3350+143del
ENST00000261584.8:c.3350+106_3350+143del	ENSP00000261584.4:n.3350+106_3350+143del
ENST00000566069.5:c.117-4089_117-4052del
ENST00000568219.5:c.2465+106_2465+143del	ENSP00000454703.2:n.2465+106_2465+143del
NM_024675.3:c.3350+106_3350+143del , LRG_308t1:c.3350+106_3350+143del	NP_078951.2:n.3350+106_3350+143del
XM_011545946.1:c.3356+106_3356+143del	XP_011544248.1:n.3356+106_3356+143del
XM_011545947.1:c.3208-4089_3208-4052del	XP_011544249.1:n.3208-4089_3208-4052del
XM_011545948.1:c.2465+106_2465+143del	XP_011544250.1:n.2465+106_2465+143del
XR_950851.1:n.4058+106_4058+143del
XM_011545946.2:c.3356+106_3356+143del	XP_011544248.1:n.3356+106_3356+143del
XM_011545947.2:c.3208-4089_3208-4052del	XP_011544249.1:n.3208-4089_3208-4052del
XM_011545948.2:c.2465+106_2465+143del	XP_011544250.1:n.2465+106_2465+143del
XM_017023671.1:c.3120-4089_3120-4052del	XP_016879160.1:n.3120-4089_3120-4052del
XM_017023672.2:c.3114-4089_3114-4052del	XP_016879161.1:n.3114-4089_3114-4052del
XM_017023673.2:c.3202-4089_3202-4052del	XP_016879162.1:n.3202-4089_3202-4052del
NM_024675.4:c.3350+106_3350+143del MANE Select	NP_078951.2:n.3350+106_3350+143del