Canonical Allele Identifier: CA2213410317
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621462A= , CM000678.2:g.23621462A= GRCh38
NC_000016.9:g.23632783A= , CM000678.1:g.23632783A= GRCh37
NC_000016.8:g.23540284A= NCBI36
NG_007406.1:g.24896T= , LRG_308:g.24896T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3019T= ENSP00000460666.3:p.Phe1007=
ENST00000565038.2:c.*494T= ENSP00000459882.2:n.*494T=
ENST00000566069.6:c.3013T= ENSP00000459237.2:p.Phe1005=
ENST00000697377.2:c.2857T= ENSP00000513286.2:p.Phe953=
ENST00000697379.2:c.3019T= ENSP00000513287.2:p.Phe1007=
ENST00000561514.2:c.2128T= ENSP00000460666.2:p.Phe710=
ENST00000697374.1:c.2128T= ENSP00000513284.1:p.Phe710=
ENST00000697375.1:n.4360T=
ENST00000697376.1:c.2128T= ENSP00000513285.1:p.Phe710=
ENST00000697377.1:c.1966T= ENSP00000513286.1:p.Phe656=
ENST00000697378.1:n.3533T=
ENST00000697379.1:c.2128T= ENSP00000513287.1:p.Phe710=
ENST00000697380.1:n.2305T=
ENST00000697381.1:n.1708T=
ENST00000697382.1:c.2128T= ENSP00000513288.1:p.Phe710=
ENST00000697383.1:c.547T= ENSP00000513289.1:p.Phe183=
ENST00000261584.9:c.3013T= MANE Select ENSP00000261584.4:p.Phe1005=
ENST00000261584.8:c.3013T= ENSP00000261584.4:p.Phe1005=
ENST00000568219.5:c.2128T= ENSP00000454703.2:p.Phe710=
NM_024675.3:c.3013T= , LRG_308t1:c.3013T= NP_078951.2:p.Phe1005=
XM_011545946.1:c.3019T= XP_011544248.1:p.Phe1007=
XM_011545947.1:c.3019T= XP_011544249.1:p.Phe1007=
XM_011545948.1:c.2128T= XP_011544250.1:p.Phe710=
XR_950851.1:n.3809T=
XM_011545946.2:c.3019T= XP_011544248.1:p.Phe1007=
XM_011545947.2:c.3019T= XP_011544249.1:p.Phe1007=
XM_011545948.2:c.2128T= XP_011544250.1:p.Phe710=
XM_017023671.1:c.3019T= XP_016879160.1:p.Phe1007=
XM_017023672.2:c.3013T= XP_016879161.1:p.Phe1005=
XM_017023673.2:c.3013T= XP_016879162.1:p.Phe1005=
NM_024675.4:c.3013T= MANE Select NP_078951.2:p.Phe1005=