Canonical Allele Identifier: CA2213410242
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621450G= , CM000678.2:g.23621450G= GRCh38
NC_000016.9:g.23632771G= , CM000678.1:g.23632771G= GRCh37
NC_000016.8:g.23540272G= NCBI36
NG_007406.1:g.24908C= , LRG_308:g.24908C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3031C= ENSP00000460666.3:p.Pro1011=
ENST00000565038.2:c.*506C= ENSP00000459882.2:n.*506C=
ENST00000566069.6:c.3025C= ENSP00000459237.2:p.Pro1009=
ENST00000697377.2:c.2869C= ENSP00000513286.2:p.Pro957=
ENST00000697379.2:c.3031C= ENSP00000513287.2:p.Pro1011=
ENST00000561514.2:c.2140C= ENSP00000460666.2:p.Pro714=
ENST00000697374.1:c.2140C= ENSP00000513284.1:p.Pro714=
ENST00000697375.1:n.4372C=
ENST00000697376.1:c.2140C= ENSP00000513285.1:p.Pro714=
ENST00000697377.1:c.1978C= ENSP00000513286.1:p.Pro660=
ENST00000697378.1:n.3545C=
ENST00000697379.1:c.2140C= ENSP00000513287.1:p.Pro714=
ENST00000697380.1:n.2317C=
ENST00000697381.1:n.1720C=
ENST00000697382.1:c.2140C= ENSP00000513288.1:p.Pro714=
ENST00000697383.1:c.559C= ENSP00000513289.1:p.Pro187=
ENST00000261584.9:c.3025C= MANE Select ENSP00000261584.4:p.Pro1009=
ENST00000261584.8:c.3025C= ENSP00000261584.4:p.Pro1009=
ENST00000568219.5:c.2140C= ENSP00000454703.2:p.Pro714=
NM_024675.3:c.3025C= , LRG_308t1:c.3025C= NP_078951.2:p.Pro1009=
XM_011545946.1:c.3031C= XP_011544248.1:p.Pro1011=
XM_011545947.1:c.3031C= XP_011544249.1:p.Pro1011=
XM_011545948.1:c.2140C= XP_011544250.1:p.Pro714=
XR_950851.1:n.3821C=
XM_011545946.2:c.3031C= XP_011544248.1:p.Pro1011=
XM_011545947.2:c.3031C= XP_011544249.1:p.Pro1011=
XM_011545948.2:c.2140C= XP_011544250.1:p.Pro714=
XM_017023671.1:c.3031C= XP_016879160.1:p.Pro1011=
XM_017023672.2:c.3025C= XP_016879161.1:p.Pro1009=
XM_017023673.2:c.3025C= XP_016879162.1:p.Pro1009=
NM_024675.4:c.3025C= MANE Select NP_078951.2:p.Pro1009=