Canonical Allele Identifier: CA395138244
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs2142254621

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23603619G>A , CM000678.2:g.23603619G>A GRCh38
NC_000016.9:g.23614940G>A , CM000678.1:g.23614940G>A GRCh37
NC_000016.8:g.23522441G>A NCBI36
NG_007406.1:g.42739C>T , LRG_308:g.42739C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000561514.3:c.3407C>T ENSP00000460666.3:p.Ser1136Phe
ENST00000565038.2:c.*886C>T ENSP00000459882.2:n.*886C>T
ENST00000566069.6:c.*36C>T ENSP00000459237.2:n.*36C>T
ENST00000697377.2:c.3245C>T ENSP00000513286.2:p.Ser1082Phe
ENST00000697379.2:c.3407C>T ENSP00000513287.2:p.Ser1136Phe
ENST00000561514.2:c.2516C>T ENSP00000460666.2:p.Ser839Phe
ENST00000697374.1:c.2516C>T ENSP00000513284.1:p.Ser839Phe
ENST00000697375.1:n.4748C>T
ENST00000697376.1:c.*36C>T ENSP00000513285.1:n.*36C>T
ENST00000697377.1:c.2354C>T ENSP00000513286.1:p.Ser785Phe
ENST00000697378.1:n.3921C>T
ENST00000697379.1:c.2516C>T ENSP00000513287.1:p.Ser839Phe
ENST00000697380.1:n.2605C>T
ENST00000697381.1:n.2096C>T
ENST00000697382.1:c.*178C>T ENSP00000513288.1:n.*178C>T
ENST00000697383.1:c.935C>T ENSP00000513289.1:p.Ser312Phe
ENST00000261584.9:c.3401C>T MANE Select ENSP00000261584.4:p.Ser1134Phe
ENST00000261584.8:c.3401C>T ENSP00000261584.4:p.Ser1134Phe
ENST00000566069.5:c.167C>T
ENST00000568219.5:c.2516C>T ENSP00000454703.2:p.Ser839Phe
NM_024675.3:c.3401C>T , LRG_308t1:c.3401C>T NP_078951.2:p.Ser1134Phe
XM_011545946.1:c.3407C>T XP_011544248.1:p.Ser1136Phe
XM_011545947.1:c.*36C>T XP_011544249.1:n.*36C>T
XM_011545948.1:c.2516C>T XP_011544250.1:p.Ser839Phe
XR_950851.1:n.4109C>T
XM_011545946.2:c.3407C>T XP_011544248.1:p.Ser1136Phe
XM_011545947.2:c.*36C>T XP_011544249.1:n.*36C>T
XM_011545948.2:c.2516C>T XP_011544250.1:p.Ser839Phe
XM_017023671.1:c.3170C>T XP_016879160.1:p.Ser1057Phe
XM_017023672.2:c.3164C>T XP_016879161.1:p.Ser1055Phe
XM_017023673.2:c.*36C>T XP_016879162.1:n.*36C>T
NM_024675.4:c.3401C>T MANE Select NP_078951.2:p.Ser1134Phe