Canonical Allele Identifier: CA395140051
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs2142274053

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23607991T>A , CM000678.2:g.23607991T>A GRCh38
NC_000016.9:g.23619312T>A , CM000678.1:g.23619312T>A GRCh37
NC_000016.8:g.23526813T>A NCBI36
NG_007406.1:g.38367A>T , LRG_308:g.38367A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3229A>T ENSP00000460666.3:p.Ser1077Cys
ENST00000565038.2:c.*704A>T ENSP00000459882.2:n.*704A>T
ENST00000566069.6:c.3202-4322A>T ENSP00000459237.2:n.3202-4322A>T
ENST00000697377.2:c.3067A>T ENSP00000513286.2:p.Ser1023Cys
ENST00000697379.2:c.3229A>T ENSP00000513287.2:p.Ser1077Cys
ENST00000561514.2:c.2338A>T ENSP00000460666.2:p.Ser780Cys
ENST00000697374.1:c.2338A>T ENSP00000513284.1:p.Ser780Cys
ENST00000697375.1:n.4570A>T
ENST00000697376.1:c.2317-4322A>T ENSP00000513285.1:n.2317-4322A>T
ENST00000697377.1:c.2176A>T ENSP00000513286.1:p.Ser726Cys
ENST00000697378.1:n.3743A>T
ENST00000697379.1:c.2338A>T ENSP00000513287.1:p.Ser780Cys
ENST00000697380.1:n.2427A>T
ENST00000697381.1:n.1918A>T
ENST00000697382.1:c.2250A>T ENSP00000513288.1:p.Ter750Cys
ENST00000697383.1:c.757A>T ENSP00000513289.1:p.Ser253Cys
ENST00000261584.9:c.3223A>T MANE Select ENSP00000261584.4:p.Ser1075Cys
ENST00000261584.8:c.3223A>T ENSP00000261584.4:p.Ser1075Cys
ENST00000566069.5:c.117-4322A>T
ENST00000568219.5:c.2338A>T ENSP00000454703.2:p.Ser780Cys
NM_024675.3:c.3223A>T , LRG_308t1:c.3223A>T NP_078951.2:p.Ser1075Cys
XM_011545946.1:c.3229A>T XP_011544248.1:p.Ser1077Cys
XM_011545947.1:c.3208-4322A>T XP_011544249.1:n.3208-4322A>T
XM_011545948.1:c.2338A>T XP_011544250.1:p.Ser780Cys
XR_950851.1:n.3931A>T
XM_011545946.2:c.3229A>T XP_011544248.1:p.Ser1077Cys
XM_011545947.2:c.3208-4322A>T XP_011544249.1:n.3208-4322A>T
XM_011545948.2:c.2338A>T XP_011544250.1:p.Ser780Cys
XM_017023671.1:c.3120-4322A>T XP_016879160.1:n.3120-4322A>T
XM_017023672.2:c.3114-4322A>T XP_016879161.1:n.3114-4322A>T
XM_017023673.2:c.3202-4322A>T XP_016879162.1:n.3202-4322A>T
NM_024675.4:c.3223A>T MANE Select NP_078951.2:p.Ser1075Cys