Canonical Allele Identifier: CA2695197590
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2674098
ClinVar RCV Id: RCV003452294

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621466_23621467delinsCCTCTGTAA , CM000678.2:g.23621466_23621467delinsCCTCTGTAA GRCh38
NC_000016.9:g.23632787_23632788delinsCCTCTGTAA , CM000678.1:g.23632787_23632788delinsCCTCTGTAA GRCh37
NC_000016.8:g.23540288_23540289delinsCCTCTGTAA NCBI36
NG_007406.1:g.24891_24892delinsTTACAGAGG , LRG_308:g.24891_24892delinsTTACAGAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3014_3015delinsTTACAGAGG ENSP00000460666.3:p.Asn1005IlefsTer10
ENST00000565038.2:c.*489_*490delinsTTACAGAGG ENSP00000459882.2:n.*489_*490delinsTTACAGAGG
ENST00000566069.6:c.3008_3009delinsTTACAGAGG ENSP00000459237.2:p.Asn1003IlefsTer10
ENST00000697377.2:c.2852_2853delinsTTACAGAGG ENSP00000513286.2:p.Asn951IlefsTer10
ENST00000697379.2:c.3014_3015delinsTTACAGAGG ENSP00000513287.2:p.Asn1005IlefsTer10
ENST00000561514.2:c.2123_2124delinsTTACAGAGG ENSP00000460666.2:p.Asn708IlefsTer10
ENST00000697374.1:c.2123_2124delinsTTACAGAGG ENSP00000513284.1:p.Asn708IlefsTer10
ENST00000697375.1:n.4355_4356delinsTTACAGAGG
ENST00000697376.1:c.2123_2124delinsTTACAGAGG ENSP00000513285.1:p.Asn708IlefsTer10
ENST00000697377.1:c.1961_1962delinsTTACAGAGG ENSP00000513286.1:p.Asn654IlefsTer10
ENST00000697378.1:n.3528_3529delinsTTACAGAGG
ENST00000697379.1:c.2123_2124delinsTTACAGAGG ENSP00000513287.1:p.Asn708IlefsTer10
ENST00000697380.1:n.2300_2301delinsTTACAGAGG
ENST00000697381.1:n.1703_1704delinsTTACAGAGG
ENST00000697382.1:c.2123_2124delinsTTACAGAGG ENSP00000513288.1:p.Asn708IlefsTer10
ENST00000697383.1:c.542_543delinsTTACAGAGG ENSP00000513289.1:p.Asn181IlefsTer10
ENST00000261584.9:c.3008_3009delinsTTACAGAGG MANE Select ENSP00000261584.4:p.Asn1003IlefsTer10
ENST00000261584.8:c.3008_3009delinsTTACAGAGG ENSP00000261584.4:p.Asn1003IlefsTer10
ENST00000568219.5:c.2123_2124delinsTTACAGAGG ENSP00000454703.2:p.Asn708IlefsTer10
NM_024675.3:c.3008_3009delinsTTACAGAGG , LRG_308t1:c.3008_3009delinsTTACAGAGG NP_078951.2:p.Asn1003IlefsTer10
XM_011545946.1:c.3014_3015delinsTTACAGAGG XP_011544248.1:p.Asn1005IlefsTer10
XM_011545947.1:c.3014_3015delinsTTACAGAGG XP_011544249.1:p.Asn1005IlefsTer10
XM_011545948.1:c.2123_2124delinsTTACAGAGG XP_011544250.1:p.Asn708IlefsTer10
XR_950851.1:n.3804_3805delinsTTACAGAGG
XM_011545946.2:c.3014_3015delinsTTACAGAGG XP_011544248.1:p.Asn1005IlefsTer10
XM_011545947.2:c.3014_3015delinsTTACAGAGG XP_011544249.1:p.Asn1005IlefsTer10
XM_011545948.2:c.2123_2124delinsTTACAGAGG XP_011544250.1:p.Asn708IlefsTer10
XM_017023671.1:c.3014_3015delinsTTACAGAGG XP_016879160.1:p.Asn1005IlefsTer10
XM_017023672.2:c.3008_3009delinsTTACAGAGG XP_016879161.1:p.Asn1003IlefsTer10
XM_017023673.2:c.3008_3009delinsTTACAGAGG XP_016879162.1:p.Asn1003IlefsTer10
NM_024675.4:c.3008_3009delinsTTACAGAGG MANE Select NP_078951.2:p.Asn1003IlefsTer10