Canonical Allele Identifier: CA395137844
Gene: PALB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23603500C>A , CM000678.2:g.23603500C>A GRCh38
NC_000016.9:g.23614821C>A , CM000678.1:g.23614821C>A GRCh37
NC_000016.8:g.23522322C>A NCBI36
NG_007406.1:g.42858G>T , LRG_308:g.42858G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000561514.3:c.3526G>T ENSP00000460666.3:p.Gly1176Ter
ENST00000565038.2:c.*1005G>T ENSP00000459882.2:n.*1005G>T
ENST00000566069.6:c.*155G>T ENSP00000459237.2:n.*155G>T
ENST00000697377.2:c.3364G>T ENSP00000513286.2:p.Gly1122Ter
ENST00000697379.2:c.3526G>T ENSP00000513287.2:p.Gly1176Ter
ENST00000561514.2:c.2635G>T ENSP00000460666.2:p.Gly879Ter
ENST00000697374.1:c.2635G>T ENSP00000513284.1:p.Gly879Ter
ENST00000697375.1:n.4867G>T
ENST00000697376.1:c.*155G>T ENSP00000513285.1:n.*155G>T
ENST00000697377.1:c.2473G>T ENSP00000513286.1:p.Gly825Ter
ENST00000697378.1:n.4040G>T
ENST00000697379.1:c.2635G>T ENSP00000513287.1:p.Gly879Ter
ENST00000697380.1:n.2724G>T
ENST00000697381.1:n.2215G>T
ENST00000697382.1:c.*297G>T ENSP00000513288.1:n.*297G>T
ENST00000697383.1:c.1054G>T ENSP00000513289.1:p.Gly352Ter
ENST00000261584.9:c.3520G>T MANE Select ENSP00000261584.4:p.Gly1174Ter
ENST00000261584.8:c.3520G>T ENSP00000261584.4:p.Gly1174Ter
ENST00000566069.5:c.286G>T
ENST00000568219.5:c.2635G>T ENSP00000454703.2:p.Gly879Ter
NM_024675.3:c.3520G>T , LRG_308t1:c.3520G>T NP_078951.2:p.Gly1174Ter
XM_011545946.1:c.3526G>T XP_011544248.1:p.Gly1176Ter
XM_011545947.1:c.*155G>T XP_011544249.1:n.*155G>T
XM_011545948.1:c.2635G>T XP_011544250.1:p.Gly879Ter
XR_950851.1:n.4228G>T
XM_011545946.2:c.3526G>T XP_011544248.1:p.Gly1176Ter
XM_011545947.2:c.*155G>T XP_011544249.1:n.*155G>T
XM_011545948.2:c.2635G>T XP_011544250.1:p.Gly879Ter
XM_017023671.1:c.3289G>T XP_016879160.1:p.Gly1097Ter
XM_017023672.2:c.3283G>T XP_016879161.1:p.Gly1095Ter
XM_017023673.2:c.*155G>T XP_016879162.1:n.*155G>T
NM_024675.4:c.3520G>T MANE Select NP_078951.2:p.Gly1174Ter