Canonical Allele Identifier: CA395133563
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs2142424566

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23635399G>C , CM000678.2:g.23635399G>C GRCh38
NC_000016.9:g.23646720G>C , CM000678.1:g.23646720G>C GRCh37
NC_000016.8:g.23554221G>C NCBI36
NG_007406.1:g.10959C>G , LRG_308:g.10959C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000561514.3:c.1153C>G ENSP00000460666.3:p.Leu385Val
ENST00000565038.2:c.211+2451C>G ENSP00000459882.2:n.211+2451C>G
ENST00000566069.6:c.1147C>G ENSP00000459237.2:p.Leu383Val
ENST00000697377.2:c.1153C>G ENSP00000513286.2:p.Leu385Val
ENST00000697379.2:c.1153C>G ENSP00000513287.2:p.Leu385Val
ENST00000561514.2:c.262C>G ENSP00000460666.2:p.Leu88Val
ENST00000697374.1:c.262C>G ENSP00000513284.1:p.Leu88Val
ENST00000697375.1:n.2494C>G
ENST00000697376.1:c.262C>G ENSP00000513285.1:p.Leu88Val
ENST00000697377.1:c.262C>G ENSP00000513286.1:p.Leu88Val
ENST00000697378.1:n.1667C>G
ENST00000697379.1:c.262C>G ENSP00000513287.1:p.Leu88Val
ENST00000697382.1:c.262C>G ENSP00000513288.1:p.Leu88Val
ENST00000697383.1:c.48+5711C>G ENSP00000513289.1:n.48+5711C>G
ENST00000697384.1:n.1301C>G
ENST00000261584.9:c.1147C>G MANE Select ENSP00000261584.4:p.Leu383Val
ENST00000261584.8:c.1147C>G ENSP00000261584.4:p.Leu383Val
ENST00000565038.1:c.86+2451C>G
ENST00000568219.5:c.262C>G ENSP00000454703.2:p.Leu88Val
NM_024675.3:c.1147C>G , LRG_308t1:c.1147C>G NP_078951.2:p.Leu383Val
XM_011545946.1:c.1153C>G XP_011544248.1:p.Leu385Val
XM_011545947.1:c.1153C>G XP_011544249.1:p.Leu385Val
XM_011545948.1:c.262C>G XP_011544250.1:p.Leu88Val
XR_950851.1:n.1943C>G
XM_011545946.2:c.1153C>G XP_011544248.1:p.Leu385Val
XM_011545947.2:c.1153C>G XP_011544249.1:p.Leu385Val
XM_011545948.2:c.262C>G XP_011544250.1:p.Leu88Val
XM_017023671.1:c.1153C>G XP_016879160.1:p.Leu385Val
XM_017023672.2:c.1147C>G XP_016879161.1:p.Leu383Val
XM_017023673.2:c.1147C>G XP_016879162.1:p.Leu383Val
NM_024675.4:c.1147C>G MANE Select NP_078951.2:p.Leu383Val