Canonical Allele Identifier: CA395131192

Gene: PALB2

Linked Data

• ClinVar Variation Id: 1773154
• ClinVar RCV Id: RCV002396728
• gnomAD v4: 16-23635086-A-C
• MyVariant Identifiers: chr16:g.23646407A>C (hg19) ; chr16:g.23635086A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635086A>C , CM000678.2:g.23635086A>C	GRCh38
NC_000016.9:g.23646407A>C , CM000678.1:g.23646407A>C	GRCh37
NC_000016.8:g.23553908A>C	NCBI36
NG_007406.1:g.11272T>G , LRG_308:g.11272T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.1466T>G	ENSP00000460666.3:p.Val489Gly
ENST00000565038.2:c.211+2764T>G	ENSP00000459882.2:n.211+2764T>G
ENST00000566069.6:c.1460T>G	ENSP00000459237.2:p.Val487Gly
ENST00000697377.2:c.1466T>G	ENSP00000513286.2:p.Val489Gly
ENST00000697379.2:c.1466T>G	ENSP00000513287.2:p.Val489Gly
ENST00000561514.2:c.575T>G	ENSP00000460666.2:p.Val192Gly
ENST00000697374.1:c.575T>G	ENSP00000513284.1:p.Val192Gly
ENST00000697375.1:n.2807T>G
ENST00000697376.1:c.575T>G	ENSP00000513285.1:p.Val192Gly
ENST00000697377.1:c.575T>G	ENSP00000513286.1:p.Val192Gly
ENST00000697378.1:n.1980T>G
ENST00000697379.1:c.575T>G	ENSP00000513287.1:p.Val192Gly
ENST00000697382.1:c.575T>G	ENSP00000513288.1:p.Val192Gly
ENST00000697383.1:c.49-5811T>G	ENSP00000513289.1:n.49-5811T>G
ENST00000697384.1:n.1614T>G
ENST00000261584.9:c.1460T>G MANE Select	ENSP00000261584.4:p.Val487Gly
ENST00000261584.8:c.1460T>G	ENSP00000261584.4:p.Val487Gly
ENST00000565038.1:c.86+2764T>G
ENST00000568219.5:c.575T>G	ENSP00000454703.2:p.Val192Gly
NM_024675.3:c.1460T>G , LRG_308t1:c.1460T>G	NP_078951.2:p.Val487Gly
XM_011545946.1:c.1466T>G	XP_011544248.1:p.Val489Gly
XM_011545947.1:c.1466T>G	XP_011544249.1:p.Val489Gly
XM_011545948.1:c.575T>G	XP_011544250.1:p.Val192Gly
XR_950851.1:n.2256T>G
XM_011545946.2:c.1466T>G	XP_011544248.1:p.Val489Gly
XM_011545947.2:c.1466T>G	XP_011544249.1:p.Val489Gly
XM_011545948.2:c.575T>G	XP_011544250.1:p.Val192Gly
XM_017023671.1:c.1466T>G	XP_016879160.1:p.Val489Gly
XM_017023672.2:c.1460T>G	XP_016879161.1:p.Val487Gly
XM_017023673.2:c.1460T>G	XP_016879162.1:p.Val487Gly
NM_024675.4:c.1460T>G MANE Select	NP_078951.2:p.Val487Gly