Canonical Allele Identifier: CA395137725
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs145598272

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23636202C>G , CM000678.2:g.23636202C>G GRCh38
NC_000016.9:g.23647523C>G , CM000678.1:g.23647523C>G GRCh37
NC_000016.8:g.23555024C>G NCBI36
NG_007406.1:g.10156G>C , LRG_308:g.10156G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.350G>C ENSP00000460666.3:p.Gly117Ala
ENST00000565038.2:c.211+1648G>C ENSP00000459882.2:n.211+1648G>C
ENST00000566069.6:c.344G>C ENSP00000459237.2:p.Gly115Ala
ENST00000697377.2:c.350G>C ENSP00000513286.2:p.Gly117Ala
ENST00000697379.2:c.350G>C ENSP00000513287.2:p.Gly117Ala
ENST00000561514.2:c.-542G>C ENSP00000460666.2:n.-542G>C
ENST00000697374.1:c.-542G>C ENSP00000513284.1:n.-542G>C
ENST00000697375.1:n.1691G>C
ENST00000697376.1:c.-542G>C ENSP00000513285.1:n.-542G>C
ENST00000697377.1:c.-542G>C ENSP00000513286.1:n.-542G>C
ENST00000697378.1:n.864G>C
ENST00000697379.1:c.-542G>C ENSP00000513287.1:n.-542G>C
ENST00000697382.1:c.-542G>C ENSP00000513288.1:n.-542G>C
ENST00000697383.1:c.48+4908G>C ENSP00000513289.1:n.48+4908G>C
ENST00000697384.1:n.498G>C
ENST00000261584.9:c.344G>C MANE Select ENSP00000261584.4:p.Gly115Ala
ENST00000261584.8:c.344G>C ENSP00000261584.4:p.Gly115Ala
ENST00000565038.1:c.86+1648G>C
ENST00000567003.1:n.622G>C
ENST00000568219.5:c.-542G>C ENSP00000454703.2:n.-542G>C
NM_024675.3:c.344G>C , LRG_308t1:c.344G>C NP_078951.2:p.Gly115Ala
XM_011545946.1:c.350G>C XP_011544248.1:p.Gly117Ala
XM_011545947.1:c.350G>C XP_011544249.1:p.Gly117Ala
XM_011545948.1:c.-542G>C XP_011544250.1:n.-542G>C
XR_950851.1:n.1140G>C
XM_011545946.2:c.350G>C XP_011544248.1:p.Gly117Ala
XM_011545947.2:c.350G>C XP_011544249.1:p.Gly117Ala
XM_011545948.2:c.-542G>C XP_011544250.1:n.-542G>C
XM_017023671.1:c.350G>C XP_016879160.1:p.Gly117Ala
XM_017023672.2:c.344G>C XP_016879161.1:p.Gly115Ala
XM_017023673.2:c.344G>C XP_016879162.1:p.Gly115Ala
NM_024675.4:c.344G>C MANE Select NP_078951.2:p.Gly115Ala