Canonical Allele Identifier: CA395144532
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs2142337865

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23623126A>C , CM000678.2:g.23623126A>C GRCh38
NC_000016.9:g.23634447A>C , CM000678.1:g.23634447A>C GRCh37
NC_000016.8:g.23541948A>C NCBI36
NG_007406.1:g.23232T>G , LRG_308:g.23232T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000561514.3:c.2845T>G ENSP00000460666.3:p.Leu949Val
ENST00000565038.2:c.*320T>G ENSP00000459882.2:n.*320T>G
ENST00000566069.6:c.2839T>G ENSP00000459237.2:p.Leu947Val
ENST00000697377.2:c.2683T>G ENSP00000513286.2:p.Leu895Val
ENST00000697379.2:c.2845T>G ENSP00000513287.2:p.Leu949Val
ENST00000561514.2:c.1954T>G ENSP00000460666.2:p.Leu652Val
ENST00000697374.1:c.1954T>G ENSP00000513284.1:p.Leu652Val
ENST00000697375.1:n.4186T>G
ENST00000697376.1:c.1954T>G ENSP00000513285.1:p.Leu652Val
ENST00000697377.1:c.1792T>G ENSP00000513286.1:p.Leu598Val
ENST00000697378.1:n.3359T>G
ENST00000697379.1:c.1954T>G ENSP00000513287.1:p.Leu652Val
ENST00000697380.1:n.2131T>G
ENST00000697381.1:n.1534T>G
ENST00000697382.1:c.1954T>G ENSP00000513288.1:p.Leu652Val
ENST00000697383.1:c.373T>G ENSP00000513289.1:p.Leu125Val
ENST00000261584.9:c.2839T>G MANE Select ENSP00000261584.4:p.Leu947Val
ENST00000261584.8:c.2839T>G ENSP00000261584.4:p.Leu947Val
ENST00000568219.5:c.1954T>G ENSP00000454703.2:p.Leu652Val
NM_024675.3:c.2839T>G , LRG_308t1:c.2839T>G NP_078951.2:p.Leu947Val
XM_011545946.1:c.2845T>G XP_011544248.1:p.Leu949Val
XM_011545947.1:c.2845T>G XP_011544249.1:p.Leu949Val
XM_011545948.1:c.1954T>G XP_011544250.1:p.Leu652Val
XR_950851.1:n.3635T>G
XM_011545946.2:c.2845T>G XP_011544248.1:p.Leu949Val
XM_011545947.2:c.2845T>G XP_011544249.1:p.Leu949Val
XM_011545948.2:c.1954T>G XP_011544250.1:p.Leu652Val
XM_017023671.1:c.2845T>G XP_016879160.1:p.Leu949Val
XM_017023672.2:c.2839T>G XP_016879161.1:p.Leu947Val
XM_017023673.2:c.2839T>G XP_016879162.1:p.Leu947Val
NM_024675.4:c.2839T>G MANE Select NP_078951.2:p.Leu947Val