Canonical Allele Identifier: CA2213409752
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621380A= , CM000678.2:g.23621380A= GRCh38
NC_000016.9:g.23632701A= , CM000678.1:g.23632701A= GRCh37
NC_000016.8:g.23540202A= NCBI36
NG_007406.1:g.24978T= , LRG_308:g.24978T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3101T= ENSP00000460666.3:p.Met1034=
ENST00000565038.2:c.*576T= ENSP00000459882.2:n.*576T=
ENST00000566069.6:c.3095T= ENSP00000459237.2:p.Met1032=
ENST00000697377.2:c.2939T= ENSP00000513286.2:p.Met980=
ENST00000697379.2:c.3101T= ENSP00000513287.2:p.Met1034=
ENST00000561514.2:c.2210T= ENSP00000460666.2:p.Met737=
ENST00000697374.1:c.2210T= ENSP00000513284.1:p.Met737=
ENST00000697375.1:n.4442T=
ENST00000697376.1:c.2210T= ENSP00000513285.1:p.Met737=
ENST00000697377.1:c.2048T= ENSP00000513286.1:p.Met683=
ENST00000697378.1:n.3615T=
ENST00000697379.1:c.2210T= ENSP00000513287.1:p.Met737=
ENST00000697380.1:n.2387T=
ENST00000697381.1:n.1790T=
ENST00000697382.1:c.2210T= ENSP00000513288.1:p.Met737=
ENST00000697383.1:c.629T= ENSP00000513289.1:p.Met210=
ENST00000261584.9:c.3095T= MANE Select ENSP00000261584.4:p.Met1032=
ENST00000261584.8:c.3095T= ENSP00000261584.4:p.Met1032=
ENST00000566069.5:c.10T=
ENST00000568219.5:c.2210T= ENSP00000454703.2:p.Met737=
NM_024675.3:c.3095T= , LRG_308t1:c.3095T= NP_078951.2:p.Met1032=
XM_011545946.1:c.3101T= XP_011544248.1:p.Met1034=
XM_011545947.1:c.3101T= XP_011544249.1:p.Met1034=
XM_011545948.1:c.2210T= XP_011544250.1:p.Met737=
XR_950851.1:n.3891T=
XM_011545946.2:c.3101T= XP_011544248.1:p.Met1034=
XM_011545947.2:c.3101T= XP_011544249.1:p.Met1034=
XM_011545948.2:c.2210T= XP_011544250.1:p.Met737=
XM_017023671.1:c.3101T= XP_016879160.1:p.Met1034=
XM_017023672.2:c.3095T= XP_016879161.1:p.Met1032=
XM_017023673.2:c.3095T= XP_016879162.1:p.Met1032=
NM_024675.4:c.3095T= MANE Select NP_078951.2:p.Met1032=