Canonical Allele Identifier: CA2213410320
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621464T= , CM000678.2:g.23621464T= GRCh38
NC_000016.9:g.23632785T= , CM000678.1:g.23632785T= GRCh37
NC_000016.8:g.23540286T= NCBI36
NG_007406.1:g.24894A= , LRG_308:g.24894A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3017A= ENSP00000460666.3:p.Gln1006=
ENST00000565038.2:c.*492A= ENSP00000459882.2:n.*492A=
ENST00000566069.6:c.3011A= ENSP00000459237.2:p.Gln1004=
ENST00000697377.2:c.2855A= ENSP00000513286.2:p.Gln952=
ENST00000697379.2:c.3017A= ENSP00000513287.2:p.Gln1006=
ENST00000561514.2:c.2126A= ENSP00000460666.2:p.Gln709=
ENST00000697374.1:c.2126A= ENSP00000513284.1:p.Gln709=
ENST00000697375.1:n.4358A=
ENST00000697376.1:c.2126A= ENSP00000513285.1:p.Gln709=
ENST00000697377.1:c.1964A= ENSP00000513286.1:p.Gln655=
ENST00000697378.1:n.3531A=
ENST00000697379.1:c.2126A= ENSP00000513287.1:p.Gln709=
ENST00000697380.1:n.2303A=
ENST00000697381.1:n.1706A=
ENST00000697382.1:c.2126A= ENSP00000513288.1:p.Gln709=
ENST00000697383.1:c.545A= ENSP00000513289.1:p.Gln182=
ENST00000261584.9:c.3011A= MANE Select ENSP00000261584.4:p.Gln1004=
ENST00000261584.8:c.3011A= ENSP00000261584.4:p.Gln1004=
ENST00000568219.5:c.2126A= ENSP00000454703.2:p.Gln709=
NM_024675.3:c.3011A= , LRG_308t1:c.3011A= NP_078951.2:p.Gln1004=
XM_011545946.1:c.3017A= XP_011544248.1:p.Gln1006=
XM_011545947.1:c.3017A= XP_011544249.1:p.Gln1006=
XM_011545948.1:c.2126A= XP_011544250.1:p.Gln709=
XR_950851.1:n.3807A=
XM_011545946.2:c.3017A= XP_011544248.1:p.Gln1006=
XM_011545947.2:c.3017A= XP_011544249.1:p.Gln1006=
XM_011545948.2:c.2126A= XP_011544250.1:p.Gln709=
XM_017023671.1:c.3017A= XP_016879160.1:p.Gln1006=
XM_017023672.2:c.3011A= XP_016879161.1:p.Gln1004=
XM_017023673.2:c.3011A= XP_016879162.1:p.Gln1004=
NM_024675.4:c.3011A= MANE Select NP_078951.2:p.Gln1004=