Canonical Allele Identifier: CA395142822
Gene: PALB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621375T>C , CM000678.2:g.23621375T>C GRCh38
NC_000016.9:g.23632696T>C , CM000678.1:g.23632696T>C GRCh37
NC_000016.8:g.23540197T>C NCBI36
NG_007406.1:g.24983A>G , LRG_308:g.24983A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3106A>G ENSP00000460666.3:p.Asn1036Asp
ENST00000565038.2:c.*581A>G ENSP00000459882.2:n.*581A>G
ENST00000566069.6:c.3100A>G ENSP00000459237.2:p.Asn1034Asp
ENST00000697377.2:c.2944A>G ENSP00000513286.2:p.Asn982Asp
ENST00000697379.2:c.3106A>G ENSP00000513287.2:p.Asn1036Asp
ENST00000561514.2:c.2215A>G ENSP00000460666.2:p.Asn739Asp
ENST00000697374.1:c.2215A>G ENSP00000513284.1:p.Asn739Asp
ENST00000697375.1:n.4447A>G
ENST00000697376.1:c.2215A>G ENSP00000513285.1:p.Asn739Asp
ENST00000697377.1:c.2053A>G ENSP00000513286.1:p.Asn685Asp
ENST00000697378.1:n.3620A>G
ENST00000697379.1:c.2215A>G ENSP00000513287.1:p.Asn739Asp
ENST00000697380.1:n.2392A>G
ENST00000697381.1:n.1795A>G
ENST00000697382.1:c.2215A>G ENSP00000513288.1:p.Asn739Asp
ENST00000697383.1:c.634A>G ENSP00000513289.1:p.Asn212Asp
ENST00000261584.9:c.3100A>G MANE Select ENSP00000261584.4:p.Asn1034Asp
ENST00000261584.8:c.3100A>G ENSP00000261584.4:p.Asn1034Asp
ENST00000566069.5:c.15A>G
ENST00000568219.5:c.2215A>G ENSP00000454703.2:p.Asn739Asp
NM_024675.3:c.3100A>G , LRG_308t1:c.3100A>G NP_078951.2:p.Asn1034Asp
XM_011545946.1:c.3106A>G XP_011544248.1:p.Asn1036Asp
XM_011545947.1:c.3106A>G XP_011544249.1:p.Asn1036Asp
XM_011545948.1:c.2215A>G XP_011544250.1:p.Asn739Asp
XR_950851.1:n.3896A>G
XM_011545946.2:c.3106A>G XP_011544248.1:p.Asn1036Asp
XM_011545947.2:c.3106A>G XP_011544249.1:p.Asn1036Asp
XM_011545948.2:c.2215A>G XP_011544250.1:p.Asn739Asp
XM_017023671.1:c.3106A>G XP_016879160.1:p.Asn1036Asp
XM_017023672.2:c.3100A>G XP_016879161.1:p.Asn1034Asp
XM_017023673.2:c.3100A>G XP_016879162.1:p.Asn1034Asp
NM_024675.4:c.3100A>G MANE Select NP_078951.2:p.Asn1034Asp