Canonical Allele Identifier: CA395138050
Gene: PALB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23603556G>T , CM000678.2:g.23603556G>T GRCh38
NC_000016.9:g.23614877G>T , CM000678.1:g.23614877G>T GRCh37
NC_000016.8:g.23522378G>T NCBI36
NG_007406.1:g.42802C>A , LRG_308:g.42802C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000561514.3:c.3470C>A ENSP00000460666.3:p.Ser1157Tyr
ENST00000565038.2:c.*949C>A ENSP00000459882.2:n.*949C>A
ENST00000566069.6:c.*99C>A ENSP00000459237.2:n.*99C>A
ENST00000697377.2:c.3308C>A ENSP00000513286.2:p.Ser1103Tyr
ENST00000697379.2:c.3470C>A ENSP00000513287.2:p.Ser1157Tyr
ENST00000561514.2:c.2579C>A ENSP00000460666.2:p.Ser860Tyr
ENST00000697374.1:c.2579C>A ENSP00000513284.1:p.Ser860Tyr
ENST00000697375.1:n.4811C>A
ENST00000697376.1:c.*99C>A ENSP00000513285.1:n.*99C>A
ENST00000697377.1:c.2417C>A ENSP00000513286.1:p.Ser806Tyr
ENST00000697378.1:n.3984C>A
ENST00000697379.1:c.2579C>A ENSP00000513287.1:p.Ser860Tyr
ENST00000697380.1:n.2668C>A
ENST00000697381.1:n.2159C>A
ENST00000697382.1:c.*241C>A ENSP00000513288.1:n.*241C>A
ENST00000697383.1:c.998C>A ENSP00000513289.1:p.Ser333Tyr
ENST00000261584.9:c.3464C>A MANE Select ENSP00000261584.4:p.Ser1155Tyr
ENST00000261584.8:c.3464C>A ENSP00000261584.4:p.Ser1155Tyr
ENST00000566069.5:c.230C>A
ENST00000568219.5:c.2579C>A ENSP00000454703.2:p.Ser860Tyr
NM_024675.3:c.3464C>A , LRG_308t1:c.3464C>A NP_078951.2:p.Ser1155Tyr
XM_011545946.1:c.3470C>A XP_011544248.1:p.Ser1157Tyr
XM_011545947.1:c.*99C>A XP_011544249.1:n.*99C>A
XM_011545948.1:c.2579C>A XP_011544250.1:p.Ser860Tyr
XR_950851.1:n.4172C>A
XM_011545946.2:c.3470C>A XP_011544248.1:p.Ser1157Tyr
XM_011545947.2:c.*99C>A XP_011544249.1:n.*99C>A
XM_011545948.2:c.2579C>A XP_011544250.1:p.Ser860Tyr
XM_017023671.1:c.3233C>A XP_016879160.1:p.Ser1078Tyr
XM_017023672.2:c.3227C>A XP_016879161.1:p.Ser1076Tyr
XM_017023673.2:c.*99C>A XP_016879162.1:n.*99C>A
NM_024675.4:c.3464C>A MANE Select NP_078951.2:p.Ser1155Tyr