Canonical Allele Identifier: CA3219202686
Community Standard Title: NM_024675.4(PALB2):c.211+34T=
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23637816A= , CM000678.2:g.23637816A= GRCh38
NC_000016.9:g.23649137A= , CM000678.1:g.23649137A= GRCh37
NC_000016.8:g.23556638A= NCBI36
NG_007406.1:g.8542T= , LRG_308:g.8542T=

Transcript Alleles

HGVS Amino-acid Change
NM_024675.4:c.211+34T= MANE Select NP_078951.2:n.211+34T=
ENST00000261584.9:c.211+34T= MANE Select ENSP00000261584.4:n.211+34T=
NM_024675.3:c.211+34T= , LRG_308t1:c.211+34T= NP_078951.2:n.211+34T=
ENST00000261584.8:c.211+34T= ENSP00000261584.4:n.211+34T=
ENST00000561514.1:c.217+34T= ENSP00000460666.1:n.217+34T=
ENST00000561514.2:c.-675+34T= ENSP00000460666.2:n.-675+34T=
ENST00000561514.3:c.217+34T= ENSP00000460666.3:n.217+34T=
ENST00000565038.1:c.86+34T=
ENST00000565038.2:c.211+34T= ENSP00000459882.2:n.211+34T=
ENST00000566069.6:c.211+34T= ENSP00000459237.2:n.211+34T=
ENST00000567003.1:n.489+34T=
ENST00000568219.5:c.-675+34T= ENSP00000454703.2:n.-675+34T=
ENST00000697374.1:c.-675+34T= ENSP00000513284.1:n.-675+34T=
ENST00000697375.1:n.1558+34T=
ENST00000697376.1:c.-675+34T= ENSP00000513285.1:n.-675+34T=
ENST00000697377.1:c.-675+34T= ENSP00000513286.1:n.-675+34T=
ENST00000697377.2:c.217+34T= ENSP00000513286.2:n.217+34T=
ENST00000697378.1:n.731+34T=
ENST00000697379.1:c.-675+34T= ENSP00000513287.1:n.-675+34T=
ENST00000697379.2:c.217+34T= ENSP00000513287.2:n.217+34T=
ENST00000697382.1:c.-675+34T= ENSP00000513288.1:n.-675+34T=
ENST00000697383.1:c.48+3294T= ENSP00000513289.1:n.48+3294T=
ENST00000697384.1:n.365+34T=
XM_011545946.1:c.217+34T= XP_011544248.1:n.217+34T=
XM_011545946.2:c.217+34T= XP_011544248.1:n.217+34T=
XM_011545947.1:c.217+34T= XP_011544249.1:n.217+34T=
XM_011545947.2:c.217+34T= XP_011544249.1:n.217+34T=
XM_011545948.1:c.-675+34T= XP_011544250.1:n.-675+34T=
XM_011545948.2:c.-675+34T= XP_011544250.1:n.-675+34T=
XM_017023671.1:c.217+34T= XP_016879160.1:n.217+34T=
XM_017023672.2:c.211+34T= XP_016879161.1:n.211+34T=
XM_017023673.2:c.211+34T= XP_016879162.1:n.211+34T=
XR_950851.1:n.1007+34T=