Canonical Allele Identifier: CA2213409822
Gene: PALB2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3091A= ENSP00000460666.3:p.Thr1031=
ENST00000565038.2:c.*566A= ENSP00000459882.2:n.*566A=
ENST00000566069.6:c.3085A= ENSP00000459237.2:p.Thr1029=
ENST00000697377.2:c.2929A= ENSP00000513286.2:p.Thr977=
ENST00000697379.2:c.3091A= ENSP00000513287.2:p.Thr1031=
ENST00000561514.2:c.2200A= ENSP00000460666.2:p.Thr734=
ENST00000697374.1:c.2200A= ENSP00000513284.1:p.Thr734=
ENST00000697375.1:n.4432A=
ENST00000697376.1:c.2200A= ENSP00000513285.1:p.Thr734=
ENST00000697377.1:c.2038A= ENSP00000513286.1:p.Thr680=
ENST00000697378.1:n.3605A=
ENST00000697379.1:c.2200A= ENSP00000513287.1:p.Thr734=
ENST00000697380.1:n.2377A=
ENST00000697381.1:n.1780A=
ENST00000697382.1:c.2200A= ENSP00000513288.1:p.Thr734=
ENST00000697383.1:c.619A= ENSP00000513289.1:p.Thr207=
ENST00000261584.9:c.3085A= MANE Select ENSP00000261584.4:p.Thr1029=
ENST00000261584.8:c.3085A= ENSP00000261584.4:p.Thr1029=
ENST00000568219.5:c.2200A= ENSP00000454703.2:p.Thr734=
NM_024675.3:c.3085A= , LRG_308t1:c.3085A= NP_078951.2:p.Thr1029=
XM_011545946.1:c.3091A= XP_011544248.1:p.Thr1031=
XM_011545947.1:c.3091A= XP_011544249.1:p.Thr1031=
XM_011545948.1:c.2200A= XP_011544250.1:p.Thr734=
XR_950851.1:n.3881A=
XM_011545946.2:c.3091A= XP_011544248.1:p.Thr1031=
XM_011545947.2:c.3091A= XP_011544249.1:p.Thr1031=
XM_011545948.2:c.2200A= XP_011544250.1:p.Thr734=
XM_017023671.1:c.3091A= XP_016879160.1:p.Thr1031=
XM_017023672.2:c.3085A= XP_016879161.1:p.Thr1029=
XM_017023673.2:c.3085A= XP_016879162.1:p.Thr1029=
NM_024675.4:c.3085A= MANE Select NP_078951.2:p.Thr1029=