Canonical Allele Identifier: CA395134096
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs878855096

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23635489T>A , CM000678.2:g.23635489T>A GRCh38
NC_000016.9:g.23646810T>A , CM000678.1:g.23646810T>A GRCh37
NC_000016.8:g.23554311T>A NCBI36
NG_007406.1:g.10869A>T , LRG_308:g.10869A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.1063A>T ENSP00000460666.3:p.Lys355Ter
ENST00000565038.2:c.211+2361A>T ENSP00000459882.2:n.211+2361A>T
ENST00000566069.6:c.1057A>T ENSP00000459237.2:p.Lys353Ter
ENST00000697377.2:c.1063A>T ENSP00000513286.2:p.Lys355Ter
ENST00000697379.2:c.1063A>T ENSP00000513287.2:p.Lys355Ter
ENST00000561514.2:c.172A>T ENSP00000460666.2:p.Lys58Ter
ENST00000697374.1:c.172A>T ENSP00000513284.1:p.Lys58Ter
ENST00000697375.1:n.2404A>T
ENST00000697376.1:c.172A>T ENSP00000513285.1:p.Lys58Ter
ENST00000697377.1:c.172A>T ENSP00000513286.1:p.Lys58Ter
ENST00000697378.1:n.1577A>T
ENST00000697379.1:c.172A>T ENSP00000513287.1:p.Lys58Ter
ENST00000697382.1:c.172A>T ENSP00000513288.1:p.Lys58Ter
ENST00000697383.1:c.48+5621A>T ENSP00000513289.1:n.48+5621A>T
ENST00000697384.1:n.1211A>T
ENST00000261584.9:c.1057A>T MANE Select ENSP00000261584.4:p.Lys353Ter
ENST00000261584.8:c.1057A>T ENSP00000261584.4:p.Lys353Ter
ENST00000565038.1:c.86+2361A>T
ENST00000568219.5:c.172A>T ENSP00000454703.2:p.Lys58Ter
NM_024675.3:c.1057A>T , LRG_308t1:c.1057A>T NP_078951.2:p.Lys353Ter
XM_011545946.1:c.1063A>T XP_011544248.1:p.Lys355Ter
XM_011545947.1:c.1063A>T XP_011544249.1:p.Lys355Ter
XM_011545948.1:c.172A>T XP_011544250.1:p.Lys58Ter
XR_950851.1:n.1853A>T
XM_011545946.2:c.1063A>T XP_011544248.1:p.Lys355Ter
XM_011545947.2:c.1063A>T XP_011544249.1:p.Lys355Ter
XM_011545948.2:c.172A>T XP_011544250.1:p.Lys58Ter
XM_017023671.1:c.1063A>T XP_016879160.1:p.Lys355Ter
XM_017023672.2:c.1057A>T XP_016879161.1:p.Lys353Ter
XM_017023673.2:c.1057A>T XP_016879162.1:p.Lys353Ter
NM_024675.4:c.1057A>T MANE Select NP_078951.2:p.Lys353Ter