Canonical Allele Identifier: CA299737
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182770
dbSNP Id: rs730881891

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23624045C>T , CM000678.2:g.23624045C>T GRCh38
NC_000016.9:g.23635366C>T , CM000678.1:g.23635366C>T GRCh37
NC_000016.8:g.23542867C>T NCBI36
NG_007406.1:g.22313G>A , LRG_308:g.22313G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.2804G>A ENSP00000460666.3:p.Cys935Tyr
ENST00000565038.2:c.*279G>A ENSP00000459882.2:n.*279G>A
ENST00000566069.6:c.2798G>A ENSP00000459237.2:p.Cys933Tyr
ENST00000697377.2:c.2642G>A ENSP00000513286.2:p.Cys881Tyr
ENST00000697379.2:c.2804G>A ENSP00000513287.2:p.Cys935Tyr
ENST00000561514.2:c.1913G>A ENSP00000460666.2:p.Cys638Tyr
ENST00000697374.1:c.1913G>A ENSP00000513284.1:p.Cys638Tyr
ENST00000697375.1:n.4145G>A
ENST00000697376.1:c.1913G>A ENSP00000513285.1:p.Cys638Tyr
ENST00000697377.1:c.1751G>A ENSP00000513286.1:p.Cys584Tyr
ENST00000697378.1:n.3318G>A
ENST00000697379.1:c.1913G>A ENSP00000513287.1:p.Cys638Tyr
ENST00000697380.1:n.2090G>A
ENST00000697381.1:n.1493G>A
ENST00000697382.1:c.1913G>A ENSP00000513288.1:p.Cys638Tyr
ENST00000697383.1:c.332G>A ENSP00000513289.1:p.Cys111Tyr
ENST00000261584.9:c.2798G>A MANE Select ENSP00000261584.4:p.Cys933Tyr
ENST00000261584.8:c.2798G>A ENSP00000261584.4:p.Cys933Tyr
ENST00000568219.5:c.1913G>A ENSP00000454703.2:p.Cys638Tyr
NM_024675.3:c.2798G>A , LRG_308t1:c.2798G>A NP_078951.2:p.Cys933Tyr
XM_011545946.1:c.2804G>A XP_011544248.1:p.Cys935Tyr
XM_011545947.1:c.2804G>A XP_011544249.1:p.Cys935Tyr
XM_011545948.1:c.1913G>A XP_011544250.1:p.Cys638Tyr
XR_950851.1:n.3594G>A
XM_011545946.2:c.2804G>A XP_011544248.1:p.Cys935Tyr
XM_011545947.2:c.2804G>A XP_011544249.1:p.Cys935Tyr
XM_011545948.2:c.1913G>A XP_011544250.1:p.Cys638Tyr
XM_017023671.1:c.2804G>A XP_016879160.1:p.Cys935Tyr
XM_017023672.2:c.2798G>A XP_016879161.1:p.Cys933Tyr
XM_017023673.2:c.2798G>A XP_016879162.1:p.Cys933Tyr
NM_024675.4:c.2798G>A MANE Select NP_078951.2:p.Cys933Tyr