Canonical Allele Identifier: CA395138249
Gene: PALB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23603620A>G , CM000678.2:g.23603620A>G GRCh38
NC_000016.9:g.23614941A>G , CM000678.1:g.23614941A>G GRCh37
NC_000016.8:g.23522442A>G NCBI36
NG_007406.1:g.42738T>C , LRG_308:g.42738T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000561514.3:c.3406T>C ENSP00000460666.3:p.Ser1136Pro
ENST00000565038.2:c.*885T>C ENSP00000459882.2:n.*885T>C
ENST00000566069.6:c.*35T>C ENSP00000459237.2:n.*35T>C
ENST00000697377.2:c.3244T>C ENSP00000513286.2:p.Ser1082Pro
ENST00000697379.2:c.3406T>C ENSP00000513287.2:p.Ser1136Pro
ENST00000561514.2:c.2515T>C ENSP00000460666.2:p.Ser839Pro
ENST00000697374.1:c.2515T>C ENSP00000513284.1:p.Ser839Pro
ENST00000697375.1:n.4747T>C
ENST00000697376.1:c.*35T>C ENSP00000513285.1:n.*35T>C
ENST00000697377.1:c.2353T>C ENSP00000513286.1:p.Ser785Pro
ENST00000697378.1:n.3920T>C
ENST00000697379.1:c.2515T>C ENSP00000513287.1:p.Ser839Pro
ENST00000697380.1:n.2604T>C
ENST00000697381.1:n.2095T>C
ENST00000697382.1:c.*177T>C ENSP00000513288.1:n.*177T>C
ENST00000697383.1:c.934T>C ENSP00000513289.1:p.Ser312Pro
ENST00000261584.9:c.3400T>C MANE Select ENSP00000261584.4:p.Ser1134Pro
ENST00000261584.8:c.3400T>C ENSP00000261584.4:p.Ser1134Pro
ENST00000566069.5:c.166T>C
ENST00000568219.5:c.2515T>C ENSP00000454703.2:p.Ser839Pro
NM_024675.3:c.3400T>C , LRG_308t1:c.3400T>C NP_078951.2:p.Ser1134Pro
XM_011545946.1:c.3406T>C XP_011544248.1:p.Ser1136Pro
XM_011545947.1:c.*35T>C XP_011544249.1:n.*35T>C
XM_011545948.1:c.2515T>C XP_011544250.1:p.Ser839Pro
XR_950851.1:n.4108T>C
XM_011545946.2:c.3406T>C XP_011544248.1:p.Ser1136Pro
XM_011545947.2:c.*35T>C XP_011544249.1:n.*35T>C
XM_011545948.2:c.2515T>C XP_011544250.1:p.Ser839Pro
XM_017023671.1:c.3169T>C XP_016879160.1:p.Ser1057Pro
XM_017023672.2:c.3163T>C XP_016879161.1:p.Ser1055Pro
XM_017023673.2:c.*35T>C XP_016879162.1:n.*35T>C
NM_024675.4:c.3400T>C MANE Select NP_078951.2:p.Ser1134Pro