Canonical Allele Identifier: CA2213409704
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621371A= , CM000678.2:g.23621371A= GRCh38
NC_000016.9:g.23632692A= , CM000678.1:g.23632692A= GRCh37
NC_000016.8:g.23540193A= NCBI36
NG_007406.1:g.24987T= , LRG_308:g.24987T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3110T= ENSP00000460666.3:p.Ile1037=
ENST00000565038.2:c.*585T= ENSP00000459882.2:n.*585T=
ENST00000566069.6:c.3104T= ENSP00000459237.2:p.Ile1035=
ENST00000697377.2:c.2948T= ENSP00000513286.2:p.Ile983=
ENST00000697379.2:c.3110T= ENSP00000513287.2:p.Ile1037=
ENST00000561514.2:c.2219T= ENSP00000460666.2:p.Ile740=
ENST00000697374.1:c.2219T= ENSP00000513284.1:p.Ile740=
ENST00000697375.1:n.4451T=
ENST00000697376.1:c.2219T= ENSP00000513285.1:p.Ile740=
ENST00000697377.1:c.2057T= ENSP00000513286.1:p.Ile686=
ENST00000697378.1:n.3624T=
ENST00000697379.1:c.2219T= ENSP00000513287.1:p.Ile740=
ENST00000697380.1:n.2396T=
ENST00000697381.1:n.1799T=
ENST00000697382.1:c.2219T= ENSP00000513288.1:p.Ile740=
ENST00000697383.1:c.638T= ENSP00000513289.1:p.Ile213=
ENST00000261584.9:c.3104T= MANE Select ENSP00000261584.4:p.Ile1035=
ENST00000261584.8:c.3104T= ENSP00000261584.4:p.Ile1035=
ENST00000566069.5:c.19T=
ENST00000568219.5:c.2219T= ENSP00000454703.2:p.Ile740=
NM_024675.3:c.3104T= , LRG_308t1:c.3104T= NP_078951.2:p.Ile1035=
XM_011545946.1:c.3110T= XP_011544248.1:p.Ile1037=
XM_011545947.1:c.3110T= XP_011544249.1:p.Ile1037=
XM_011545948.1:c.2219T= XP_011544250.1:p.Ile740=
XR_950851.1:n.3900T=
XM_011545946.2:c.3110T= XP_011544248.1:p.Ile1037=
XM_011545947.2:c.3110T= XP_011544249.1:p.Ile1037=
XM_011545948.2:c.2219T= XP_011544250.1:p.Ile740=
XM_017023671.1:c.3110T= XP_016879160.1:p.Ile1037=
XM_017023672.2:c.3104T= XP_016879161.1:p.Ile1035=
XM_017023673.2:c.3104T= XP_016879162.1:p.Ile1035=
NM_024675.4:c.3104T= MANE Select NP_078951.2:p.Ile1035=