Canonical Allele Identifier: CA395134551
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 578696
dbSNP Id: rs1060502774

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23635540T>G , CM000678.2:g.23635540T>G GRCh38
NC_000016.9:g.23646861T>G , CM000678.1:g.23646861T>G GRCh37
NC_000016.8:g.23554362T>G NCBI36
NG_007406.1:g.10818A>C , LRG_308:g.10818A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.1012A>C ENSP00000460666.3:p.Asn338His
ENST00000565038.2:c.211+2310A>C ENSP00000459882.2:n.211+2310A>C
ENST00000566069.6:c.1006A>C ENSP00000459237.2:p.Asn336His
ENST00000697377.2:c.1012A>C ENSP00000513286.2:p.Asn338His
ENST00000697379.2:c.1012A>C ENSP00000513287.2:p.Asn338His
ENST00000561514.2:c.121A>C ENSP00000460666.2:p.Asn41His
ENST00000697374.1:c.121A>C ENSP00000513284.1:p.Asn41His
ENST00000697375.1:n.2353A>C
ENST00000697376.1:c.121A>C ENSP00000513285.1:p.Asn41His
ENST00000697377.1:c.121A>C ENSP00000513286.1:p.Asn41His
ENST00000697378.1:n.1526A>C
ENST00000697379.1:c.121A>C ENSP00000513287.1:p.Asn41His
ENST00000697382.1:c.121A>C ENSP00000513288.1:p.Asn41His
ENST00000697383.1:c.48+5570A>C ENSP00000513289.1:n.48+5570A>C
ENST00000697384.1:n.1160A>C
ENST00000261584.9:c.1006A>C MANE Select ENSP00000261584.4:p.Asn336His
ENST00000261584.8:c.1006A>C ENSP00000261584.4:p.Asn336His
ENST00000565038.1:c.86+2310A>C
ENST00000568219.5:c.121A>C ENSP00000454703.2:p.Asn41His
NM_024675.3:c.1006A>C , LRG_308t1:c.1006A>C NP_078951.2:p.Asn336His
XM_011545946.1:c.1012A>C XP_011544248.1:p.Asn338His
XM_011545947.1:c.1012A>C XP_011544249.1:p.Asn338His
XM_011545948.1:c.121A>C XP_011544250.1:p.Asn41His
XR_950851.1:n.1802A>C
XM_011545946.2:c.1012A>C XP_011544248.1:p.Asn338His
XM_011545947.2:c.1012A>C XP_011544249.1:p.Asn338His
XM_011545948.2:c.121A>C XP_011544250.1:p.Asn41His
XM_017023671.1:c.1012A>C XP_016879160.1:p.Asn338His
XM_017023672.2:c.1006A>C XP_016879161.1:p.Asn336His
XM_017023673.2:c.1006A>C XP_016879162.1:p.Asn336His
NM_024675.4:c.1006A>C MANE Select NP_078951.2:p.Asn336His