Canonical Allele Identifier: CA2213422992
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23629977G= , CM000678.2:g.23629977G= GRCh38
NC_000016.9:g.23641298G= , CM000678.1:g.23641298G= GRCh37
NC_000016.8:g.23548799G= NCBI36
NG_007406.1:g.16381C= , LRG_308:g.16381C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.2183C= ENSP00000460666.3:p.Pro728=
ENST00000565038.2:c.212-702C= ENSP00000459882.2:n.212-702C=
ENST00000566069.6:c.2177C= ENSP00000459237.2:p.Pro726=
ENST00000697377.2:c.2183C= ENSP00000513286.2:p.Pro728=
ENST00000697379.2:c.2183C= ENSP00000513287.2:p.Pro728=
ENST00000561514.2:c.1292C= ENSP00000460666.2:p.Pro431=
ENST00000697374.1:c.1292C= ENSP00000513284.1:p.Pro431=
ENST00000697375.1:n.3524C=
ENST00000697376.1:c.1292C= ENSP00000513285.1:p.Pro431=
ENST00000697377.1:c.1292C= ENSP00000513286.1:p.Pro431=
ENST00000697378.1:n.2697C=
ENST00000697379.1:c.1292C= ENSP00000513287.1:p.Pro431=
ENST00000697380.1:n.1105C=
ENST00000697381.1:n.872C=
ENST00000697382.1:c.1292C= ENSP00000513288.1:p.Pro431=
ENST00000697383.1:c.49-702C= ENSP00000513289.1:n.49-702C=
ENST00000697384.1:n.2331C=
ENST00000261584.9:c.2177C= MANE Select ENSP00000261584.4:p.Pro726=
ENST00000261584.8:c.2177C= ENSP00000261584.4:p.Pro726=
ENST00000565038.1:c.87-702C=
ENST00000568219.5:c.1292C= ENSP00000454703.2:p.Pro431=
NM_024675.3:c.2177C= , LRG_308t1:c.2177C= NP_078951.2:p.Pro726=
XM_011545946.1:c.2183C= XP_011544248.1:p.Pro728=
XM_011545947.1:c.2183C= XP_011544249.1:p.Pro728=
XM_011545948.1:c.1292C= XP_011544250.1:p.Pro431=
XR_950851.1:n.2973C=
XM_011545946.2:c.2183C= XP_011544248.1:p.Pro728=
XM_011545947.2:c.2183C= XP_011544249.1:p.Pro728=
XM_011545948.2:c.1292C= XP_011544250.1:p.Pro431=
XM_017023671.1:c.2183C= XP_016879160.1:p.Pro728=
XM_017023672.2:c.2177C= XP_016879161.1:p.Pro726=
XM_017023673.2:c.2177C= XP_016879162.1:p.Pro726=
NM_024675.4:c.2177C= MANE Select NP_078951.2:p.Pro726=