Canonical Allele Identifier: CA2213432380
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23636252G= , CM000678.2:g.23636252G= GRCh38
NC_000016.9:g.23647573G= , CM000678.1:g.23647573G= GRCh37
NC_000016.8:g.23555074G= NCBI36
NG_007406.1:g.10106C= , LRG_308:g.10106C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.300C= ENSP00000460666.3:p.Ile100=
ENST00000565038.2:c.211+1598C= ENSP00000459882.2:n.211+1598C=
ENST00000566069.6:c.294C= ENSP00000459237.2:p.Ile98=
ENST00000697377.2:c.300C= ENSP00000513286.2:p.Ile100=
ENST00000697379.2:c.300C= ENSP00000513287.2:p.Ile100=
ENST00000561514.2:c.-592C= ENSP00000460666.2:n.-592C=
ENST00000697374.1:c.-592C= ENSP00000513284.1:n.-592C=
ENST00000697375.1:n.1641C=
ENST00000697376.1:c.-592C= ENSP00000513285.1:n.-592C=
ENST00000697377.1:c.-592C= ENSP00000513286.1:n.-592C=
ENST00000697378.1:n.814C=
ENST00000697379.1:c.-592C= ENSP00000513287.1:n.-592C=
ENST00000697382.1:c.-592C= ENSP00000513288.1:n.-592C=
ENST00000697383.1:c.48+4858C= ENSP00000513289.1:n.48+4858C=
ENST00000697384.1:n.448C=
ENST00000261584.9:c.294C= MANE Select ENSP00000261584.4:p.Ile98=
ENST00000261584.8:c.294C= ENSP00000261584.4:p.Ile98=
ENST00000565038.1:c.86+1598C=
ENST00000567003.1:n.572C=
ENST00000568219.5:c.-592C= ENSP00000454703.2:n.-592C=
NM_024675.3:c.294C= , LRG_308t1:c.294C= NP_078951.2:p.Ile98=
XM_011545946.1:c.300C= XP_011544248.1:p.Ile100=
XM_011545947.1:c.300C= XP_011544249.1:p.Ile100=
XM_011545948.1:c.-592C= XP_011544250.1:n.-592C=
XR_950851.1:n.1090C=
XM_011545946.2:c.300C= XP_011544248.1:p.Ile100=
XM_011545947.2:c.300C= XP_011544249.1:p.Ile100=
XM_011545948.2:c.-592C= XP_011544250.1:n.-592C=
XM_017023671.1:c.300C= XP_016879160.1:p.Ile100=
XM_017023672.2:c.294C= XP_016879161.1:p.Ile98=
XM_017023673.2:c.294C= XP_016879162.1:p.Ile98=
NM_024675.4:c.294C= MANE Select NP_078951.2:p.Ile98=