Canonical Allele Identifier: CA2632328125

Gene: PALB2

Linked Data

• gnomAD v4: 16-23636392-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23636392_23636393insG , CM000678.2:g.23636392_23636393insG	GRCh38
NC_000016.9:g.23647713_23647714insG , CM000678.1:g.23647713_23647714insG	GRCh37
NC_000016.8:g.23555214_23555215insG	NCBI36
NG_007406.1:g.9965_9966insC , LRG_308:g.9965_9966insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.218-59_218-58insC	ENSP00000460666.3:n.218-59_218-58insC
ENST00000565038.2:c.211+1457_211+1458insC	ENSP00000459882.2:n.211+1457_211+1458insC
ENST00000566069.6:c.212-59_212-58insC	ENSP00000459237.2:n.212-59_212-58insC
ENST00000697377.2:c.218-59_218-58insC	ENSP00000513286.2:n.218-59_218-58insC
ENST00000697379.2:c.218-59_218-58insC	ENSP00000513287.2:n.218-59_218-58insC
ENST00000561514.2:c.-674-59_-674-58insC	ENSP00000460666.2:n.-674-59_-674-58insC
ENST00000697374.1:c.-674-59_-674-58insC	ENSP00000513284.1:n.-674-59_-674-58insC
ENST00000697375.1:n.1559-59_1559-58insC
ENST00000697376.1:c.-674-59_-674-58insC	ENSP00000513285.1:n.-674-59_-674-58insC
ENST00000697377.1:c.-674-59_-674-58insC	ENSP00000513286.1:n.-674-59_-674-58insC
ENST00000697378.1:n.732-59_732-58insC
ENST00000697379.1:c.-674-59_-674-58insC	ENSP00000513287.1:n.-674-59_-674-58insC
ENST00000697382.1:c.-674-59_-674-58insC	ENSP00000513288.1:n.-674-59_-674-58insC
ENST00000697383.1:c.48+4717_48+4718insC	ENSP00000513289.1:n.48+4717_48+4718insC
ENST00000697384.1:n.366-59_366-58insC
ENST00000261584.9:c.212-59_212-58insC MANE Select	ENSP00000261584.4:n.212-59_212-58insC
ENST00000261584.8:c.212-59_212-58insC	ENSP00000261584.4:n.212-59_212-58insC
ENST00000561514.1:c.218-59_218-58insC	ENSP00000460666.1:n.218-59_218-58insC
ENST00000565038.1:c.86+1457_86+1458insC
ENST00000567003.1:n.490-59_490-58insC
ENST00000568219.5:c.-674-59_-674-58insC	ENSP00000454703.2:n.-674-59_-674-58insC
NM_024675.3:c.212-59_212-58insC , LRG_308t1:c.212-59_212-58insC	NP_078951.2:n.212-59_212-58insC
XM_011545946.1:c.218-59_218-58insC	XP_011544248.1:n.218-59_218-58insC
XM_011545947.1:c.218-59_218-58insC	XP_011544249.1:n.218-59_218-58insC
XM_011545948.1:c.-674-59_-674-58insC	XP_011544250.1:n.-674-59_-674-58insC
XR_950851.1:n.1008-59_1008-58insC
XM_011545946.2:c.218-59_218-58insC	XP_011544248.1:n.218-59_218-58insC
XM_011545947.2:c.218-59_218-58insC	XP_011544249.1:n.218-59_218-58insC
XM_011545948.2:c.-674-59_-674-58insC	XP_011544250.1:n.-674-59_-674-58insC
XM_017023671.1:c.218-59_218-58insC	XP_016879160.1:n.218-59_218-58insC
XM_017023672.2:c.212-59_212-58insC	XP_016879161.1:n.212-59_212-58insC
XM_017023673.2:c.212-59_212-58insC	XP_016879162.1:n.212-59_212-58insC
NM_024675.4:c.212-59_212-58insC MANE Select	NP_078951.2:n.212-59_212-58insC