Canonical Allele Identifier: CA2213409950
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621412C= , CM000678.2:g.23621412C= GRCh38
NC_000016.9:g.23632733C= , CM000678.1:g.23632733C= GRCh37
NC_000016.8:g.23540234C= NCBI36
NG_007406.1:g.24946G= , LRG_308:g.24946G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3069G= ENSP00000460666.3:p.Gly1023=
ENST00000565038.2:c.*544G= ENSP00000459882.2:n.*544G=
ENST00000566069.6:c.3063G= ENSP00000459237.2:p.Gly1021=
ENST00000697377.2:c.2907G= ENSP00000513286.2:p.Gly969=
ENST00000697379.2:c.3069G= ENSP00000513287.2:p.Gly1023=
ENST00000561514.2:c.2178G= ENSP00000460666.2:p.Gly726=
ENST00000697374.1:c.2178G= ENSP00000513284.1:p.Gly726=
ENST00000697375.1:n.4410G=
ENST00000697376.1:c.2178G= ENSP00000513285.1:p.Gly726=
ENST00000697377.1:c.2016G= ENSP00000513286.1:p.Gly672=
ENST00000697378.1:n.3583G=
ENST00000697379.1:c.2178G= ENSP00000513287.1:p.Gly726=
ENST00000697380.1:n.2355G=
ENST00000697381.1:n.1758G=
ENST00000697382.1:c.2178G= ENSP00000513288.1:p.Gly726=
ENST00000697383.1:c.597G= ENSP00000513289.1:p.Gly199=
ENST00000261584.9:c.3063G= MANE Select ENSP00000261584.4:p.Gly1021=
ENST00000261584.8:c.3063G= ENSP00000261584.4:p.Gly1021=
ENST00000568219.5:c.2178G= ENSP00000454703.2:p.Gly726=
NM_024675.3:c.3063G= , LRG_308t1:c.3063G= NP_078951.2:p.Gly1021=
XM_011545946.1:c.3069G= XP_011544248.1:p.Gly1023=
XM_011545947.1:c.3069G= XP_011544249.1:p.Gly1023=
XM_011545948.1:c.2178G= XP_011544250.1:p.Gly726=
XR_950851.1:n.3859G=
XM_011545946.2:c.3069G= XP_011544248.1:p.Gly1023=
XM_011545947.2:c.3069G= XP_011544249.1:p.Gly1023=
XM_011545948.2:c.2178G= XP_011544250.1:p.Gly726=
XM_017023671.1:c.3069G= XP_016879160.1:p.Gly1023=
XM_017023672.2:c.3063G= XP_016879161.1:p.Gly1021=
XM_017023673.2:c.3063G= XP_016879162.1:p.Gly1021=
NM_024675.4:c.3063G= MANE Select NP_078951.2:p.Gly1021=