Canonical Allele Identifier: CA395142812
Gene: PALB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621373G>T , CM000678.2:g.23621373G>T GRCh38
NC_000016.9:g.23632694G>T , CM000678.1:g.23632694G>T GRCh37
NC_000016.8:g.23540195G>T NCBI36
NG_007406.1:g.24985C>A , LRG_308:g.24985C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3108C>A ENSP00000460666.3:p.Asn1036Lys
ENST00000565038.2:c.*583C>A ENSP00000459882.2:n.*583C>A
ENST00000566069.6:c.3102C>A ENSP00000459237.2:p.Asn1034Lys
ENST00000697377.2:c.2946C>A ENSP00000513286.2:p.Asn982Lys
ENST00000697379.2:c.3108C>A ENSP00000513287.2:p.Asn1036Lys
ENST00000561514.2:c.2217C>A ENSP00000460666.2:p.Asn739Lys
ENST00000697374.1:c.2217C>A ENSP00000513284.1:p.Asn739Lys
ENST00000697375.1:n.4449C>A
ENST00000697376.1:c.2217C>A ENSP00000513285.1:p.Asn739Lys
ENST00000697377.1:c.2055C>A ENSP00000513286.1:p.Asn685Lys
ENST00000697378.1:n.3622C>A
ENST00000697379.1:c.2217C>A ENSP00000513287.1:p.Asn739Lys
ENST00000697380.1:n.2394C>A
ENST00000697381.1:n.1797C>A
ENST00000697382.1:c.2217C>A ENSP00000513288.1:p.Asn739Lys
ENST00000697383.1:c.636C>A ENSP00000513289.1:p.Asn212Lys
ENST00000261584.9:c.3102C>A MANE Select ENSP00000261584.4:p.Asn1034Lys
ENST00000261584.8:c.3102C>A ENSP00000261584.4:p.Asn1034Lys
ENST00000566069.5:c.17C>A
ENST00000568219.5:c.2217C>A ENSP00000454703.2:p.Asn739Lys
NM_024675.3:c.3102C>A , LRG_308t1:c.3102C>A NP_078951.2:p.Asn1034Lys
XM_011545946.1:c.3108C>A XP_011544248.1:p.Asn1036Lys
XM_011545947.1:c.3108C>A XP_011544249.1:p.Asn1036Lys
XM_011545948.1:c.2217C>A XP_011544250.1:p.Asn739Lys
XR_950851.1:n.3898C>A
XM_011545946.2:c.3108C>A XP_011544248.1:p.Asn1036Lys
XM_011545947.2:c.3108C>A XP_011544249.1:p.Asn1036Lys
XM_011545948.2:c.2217C>A XP_011544250.1:p.Asn739Lys
XM_017023671.1:c.3108C>A XP_016879160.1:p.Asn1036Lys
XM_017023672.2:c.3102C>A XP_016879161.1:p.Asn1034Lys
XM_017023673.2:c.3102C>A XP_016879162.1:p.Asn1034Lys
NM_024675.4:c.3102C>A MANE Select NP_078951.2:p.Asn1034Lys