Canonical Allele Identifier: CA395142892
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs1567212837

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621390T>A , CM000678.2:g.23621390T>A GRCh38
NC_000016.9:g.23632711T>A , CM000678.1:g.23632711T>A GRCh37
NC_000016.8:g.23540212T>A NCBI36
NG_007406.1:g.24968A>T , LRG_308:g.24968A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3091A>T ENSP00000460666.3:p.Thr1031Ser
ENST00000565038.2:c.*566A>T ENSP00000459882.2:n.*566A>T
ENST00000566069.6:c.3085A>T ENSP00000459237.2:p.Thr1029Ser
ENST00000697377.2:c.2929A>T ENSP00000513286.2:p.Thr977Ser
ENST00000697379.2:c.3091A>T ENSP00000513287.2:p.Thr1031Ser
ENST00000561514.2:c.2200A>T ENSP00000460666.2:p.Thr734Ser
ENST00000697374.1:c.2200A>T ENSP00000513284.1:p.Thr734Ser
ENST00000697375.1:n.4432A>T
ENST00000697376.1:c.2200A>T ENSP00000513285.1:p.Thr734Ser
ENST00000697377.1:c.2038A>T ENSP00000513286.1:p.Thr680Ser
ENST00000697378.1:n.3605A>T
ENST00000697379.1:c.2200A>T ENSP00000513287.1:p.Thr734Ser
ENST00000697380.1:n.2377A>T
ENST00000697381.1:n.1780A>T
ENST00000697382.1:c.2200A>T ENSP00000513288.1:p.Thr734Ser
ENST00000697383.1:c.619A>T ENSP00000513289.1:p.Thr207Ser
ENST00000261584.9:c.3085A>T MANE Select ENSP00000261584.4:p.Thr1029Ser
ENST00000261584.8:c.3085A>T ENSP00000261584.4:p.Thr1029Ser
ENST00000568219.5:c.2200A>T ENSP00000454703.2:p.Thr734Ser
NM_024675.3:c.3085A>T , LRG_308t1:c.3085A>T NP_078951.2:p.Thr1029Ser
XM_011545946.1:c.3091A>T XP_011544248.1:p.Thr1031Ser
XM_011545947.1:c.3091A>T XP_011544249.1:p.Thr1031Ser
XM_011545948.1:c.2200A>T XP_011544250.1:p.Thr734Ser
XR_950851.1:n.3881A>T
XM_011545946.2:c.3091A>T XP_011544248.1:p.Thr1031Ser
XM_011545947.2:c.3091A>T XP_011544249.1:p.Thr1031Ser
XM_011545948.2:c.2200A>T XP_011544250.1:p.Thr734Ser
XM_017023671.1:c.3091A>T XP_016879160.1:p.Thr1031Ser
XM_017023672.2:c.3085A>T XP_016879161.1:p.Thr1029Ser
XM_017023673.2:c.3085A>T XP_016879162.1:p.Thr1029Ser
NM_024675.4:c.3085A>T MANE Select NP_078951.2:p.Thr1029Ser