Canonical Allele Identifier: CA395138812
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs1064793902

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23636251T>A , CM000678.2:g.23636251T>A GRCh38
NC_000016.9:g.23647572T>A , CM000678.1:g.23647572T>A GRCh37
NC_000016.8:g.23555073T>A NCBI36
NG_007406.1:g.10107A>T , LRG_308:g.10107A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.301A>T ENSP00000460666.3:p.Thr101Ser
ENST00000565038.2:c.211+1599A>T ENSP00000459882.2:n.211+1599A>T
ENST00000566069.6:c.295A>T ENSP00000459237.2:p.Thr99Ser
ENST00000697377.2:c.301A>T ENSP00000513286.2:p.Thr101Ser
ENST00000697379.2:c.301A>T ENSP00000513287.2:p.Thr101Ser
ENST00000561514.2:c.-591A>T ENSP00000460666.2:n.-591A>T
ENST00000697374.1:c.-591A>T ENSP00000513284.1:n.-591A>T
ENST00000697375.1:n.1642A>T
ENST00000697376.1:c.-591A>T ENSP00000513285.1:n.-591A>T
ENST00000697377.1:c.-591A>T ENSP00000513286.1:n.-591A>T
ENST00000697378.1:n.815A>T
ENST00000697379.1:c.-591A>T ENSP00000513287.1:n.-591A>T
ENST00000697382.1:c.-591A>T ENSP00000513288.1:n.-591A>T
ENST00000697383.1:c.48+4859A>T ENSP00000513289.1:n.48+4859A>T
ENST00000697384.1:n.449A>T
ENST00000261584.9:c.295A>T MANE Select ENSP00000261584.4:p.Thr99Ser
ENST00000261584.8:c.295A>T ENSP00000261584.4:p.Thr99Ser
ENST00000565038.1:c.86+1599A>T
ENST00000567003.1:n.573A>T
ENST00000568219.5:c.-591A>T ENSP00000454703.2:n.-591A>T
NM_024675.3:c.295A>T , LRG_308t1:c.295A>T NP_078951.2:p.Thr99Ser
XM_011545946.1:c.301A>T XP_011544248.1:p.Thr101Ser
XM_011545947.1:c.301A>T XP_011544249.1:p.Thr101Ser
XM_011545948.1:c.-591A>T XP_011544250.1:n.-591A>T
XR_950851.1:n.1091A>T
XM_011545946.2:c.301A>T XP_011544248.1:p.Thr101Ser
XM_011545947.2:c.301A>T XP_011544249.1:p.Thr101Ser
XM_011545948.2:c.-591A>T XP_011544250.1:n.-591A>T
XM_017023671.1:c.301A>T XP_016879160.1:p.Thr101Ser
XM_017023672.2:c.295A>T XP_016879161.1:p.Thr99Ser
XM_017023673.2:c.295A>T XP_016879162.1:p.Thr99Ser
NM_024675.4:c.295A>T MANE Select NP_078951.2:p.Thr99Ser