Canonical Allele Identifier: CA2580091264
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1727677
ClinVar RCV Id: RCV002326017
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621334_23621370dup , CM000678.2:g.23621334_23621370dup GRCh38
NC_000016.9:g.23632655_23632691dup , CM000678.1:g.23632655_23632691dup GRCh37
NC_000016.8:g.23540156_23540192dup NCBI36
NG_007406.1:g.24988_25024dup , LRG_308:g.24988_25024dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3111_3119+28dup
ENST00000565038.2:c.*586_*594+28dup
ENST00000566069.6:c.3105_3113+28dup
ENST00000697377.2:c.2949_2957+28dup
ENST00000697379.2:c.3111_3119+28dup
ENST00000561514.2:c.2220_2228+28dup
ENST00000697374.1:c.2220_2228+28dup
ENST00000697375.1:n.4452_4460+28dup
ENST00000697376.1:c.2220_2228+28dup
ENST00000697377.1:c.2058_2066+28dup
ENST00000697378.1:n.3625_3633+28dup
ENST00000697379.1:c.2220_2228+28dup
ENST00000697380.1:n.2397_2405+28dup
ENST00000697381.1:n.1800_1808+28dup
ENST00000697382.1:c.2220_2228+28dup
ENST00000697383.1:c.639_647+28dup
ENST00000261584.9:c.3105_3113+28dup
ENST00000261584.8:c.3105_3113+28dup
ENST00000566069.5:c.20_28+28dup
ENST00000568219.5:c.2220_2228+28dup
NM_024675.3:c.3105_3113+28dup , LRG_308t1:c.3105_3113+28dup
XM_011545946.1:c.3111_3119+28dup
XM_011545947.1:c.3111_3119+28dup
XM_011545948.1:c.2220_2228+28dup
XR_950851.1:n.3901_3909+28dup
XM_011545946.2:c.3111_3119+28dup
XM_011545947.2:c.3111_3119+28dup
XM_011545948.2:c.2220_2228+28dup
XM_017023671.1:c.3111_3119+28dup
XM_017023672.2:c.3105_3113+28dup
XM_017023673.2:c.3105_3113+28dup
NM_024675.4:c.3105_3113+28dup
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