Canonical Allele Identifier: CA395143201
Gene: PALB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621470T>G , CM000678.2:g.23621470T>G GRCh38
NC_000016.9:g.23632791T>G , CM000678.1:g.23632791T>G GRCh37
NC_000016.8:g.23540292T>G NCBI36
NG_007406.1:g.24888A>C , LRG_308:g.24888A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3011A>C ENSP00000460666.3:p.Glu1004Ala
ENST00000565038.2:c.*486A>C ENSP00000459882.2:n.*486A>C
ENST00000566069.6:c.3005A>C ENSP00000459237.2:p.Glu1002Ala
ENST00000697377.2:c.2849A>C ENSP00000513286.2:p.Glu950Ala
ENST00000697379.2:c.3011A>C ENSP00000513287.2:p.Glu1004Ala
ENST00000561514.2:c.2120A>C ENSP00000460666.2:p.Glu707Ala
ENST00000697374.1:c.2120A>C ENSP00000513284.1:p.Glu707Ala
ENST00000697375.1:n.4352A>C
ENST00000697376.1:c.2120A>C ENSP00000513285.1:p.Glu707Ala
ENST00000697377.1:c.1958A>C ENSP00000513286.1:p.Glu653Ala
ENST00000697378.1:n.3525A>C
ENST00000697379.1:c.2120A>C ENSP00000513287.1:p.Glu707Ala
ENST00000697380.1:n.2297A>C
ENST00000697381.1:n.1700A>C
ENST00000697382.1:c.2120A>C ENSP00000513288.1:p.Glu707Ala
ENST00000697383.1:c.539A>C ENSP00000513289.1:p.Glu180Ala
ENST00000261584.9:c.3005A>C MANE Select ENSP00000261584.4:p.Glu1002Ala
ENST00000261584.8:c.3005A>C ENSP00000261584.4:p.Glu1002Ala
ENST00000568219.5:c.2120A>C ENSP00000454703.2:p.Glu707Ala
NM_024675.3:c.3005A>C , LRG_308t1:c.3005A>C NP_078951.2:p.Glu1002Ala
XM_011545946.1:c.3011A>C XP_011544248.1:p.Glu1004Ala
XM_011545947.1:c.3011A>C XP_011544249.1:p.Glu1004Ala
XM_011545948.1:c.2120A>C XP_011544250.1:p.Glu707Ala
XR_950851.1:n.3801A>C
XM_011545946.2:c.3011A>C XP_011544248.1:p.Glu1004Ala
XM_011545947.2:c.3011A>C XP_011544249.1:p.Glu1004Ala
XM_011545948.2:c.2120A>C XP_011544250.1:p.Glu707Ala
XM_017023671.1:c.3011A>C XP_016879160.1:p.Glu1004Ala
XM_017023672.2:c.3005A>C XP_016879161.1:p.Glu1002Ala
XM_017023673.2:c.3005A>C XP_016879162.1:p.Glu1002Ala
NM_024675.4:c.3005A>C MANE Select NP_078951.2:p.Glu1002Ala