Canonical Allele Identifier: CA395127515

Gene: PALB2

Linked Data

• ClinVar Variation Id: 618260
• ClinVar RCV Id: RCV000756460 ; RCV002406678 ; RCV003453539
• dbSNP Id: rs760094988
• gnomAD v4: 16-23630235-G-C
• MyVariant Identifiers: chr16:g.23641556G>C (hg19) ; chr16:g.23630235G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23630235G>C , CM000678.2:g.23630235G>C	GRCh38
NC_000016.9:g.23641556G>C , CM000678.1:g.23641556G>C	GRCh37
NC_000016.8:g.23549057G>C	NCBI36
NG_007406.1:g.16123C>G , LRG_308:g.16123C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1925C>G	ENSP00000460666.3:p.Ser642Ter
ENST00000565038.2:c.212-960C>G	ENSP00000459882.2:n.212-960C>G
ENST00000566069.6:c.1919C>G	ENSP00000459237.2:p.Ser640Ter
ENST00000697377.2:c.1925C>G	ENSP00000513286.2:p.Ser642Ter
ENST00000697379.2:c.1925C>G	ENSP00000513287.2:p.Ser642Ter
ENST00000561514.2:c.1034C>G	ENSP00000460666.2:p.Ser345Ter
ENST00000697374.1:c.1034C>G	ENSP00000513284.1:p.Ser345Ter
ENST00000697375.1:n.3266C>G
ENST00000697376.1:c.1034C>G	ENSP00000513285.1:p.Ser345Ter
ENST00000697377.1:c.1034C>G	ENSP00000513286.1:p.Ser345Ter
ENST00000697378.1:n.2439C>G
ENST00000697379.1:c.1034C>G	ENSP00000513287.1:p.Ser345Ter
ENST00000697380.1:n.847C>G
ENST00000697381.1:n.614C>G
ENST00000697382.1:c.1034C>G	ENSP00000513288.1:p.Ser345Ter
ENST00000697383.1:c.49-960C>G	ENSP00000513289.1:n.49-960C>G
ENST00000697384.1:n.2073C>G
ENST00000261584.9:c.1919C>G MANE Select	ENSP00000261584.4:p.Ser640Ter
ENST00000261584.8:c.1919C>G	ENSP00000261584.4:p.Ser640Ter
ENST00000565038.1:c.87-960C>G
ENST00000568219.5:c.1034C>G	ENSP00000454703.2:p.Ser345Ter
NM_024675.3:c.1919C>G , LRG_308t1:c.1919C>G	NP_078951.2:p.Ser640Ter
XM_011545946.1:c.1925C>G	XP_011544248.1:p.Ser642Ter
XM_011545947.1:c.1925C>G	XP_011544249.1:p.Ser642Ter
XM_011545948.1:c.1034C>G	XP_011544250.1:p.Ser345Ter
XR_950851.1:n.2715C>G
XM_011545946.2:c.1925C>G	XP_011544248.1:p.Ser642Ter
XM_011545947.2:c.1925C>G	XP_011544249.1:p.Ser642Ter
XM_011545948.2:c.1034C>G	XP_011544250.1:p.Ser345Ter
XM_017023671.1:c.1925C>G	XP_016879160.1:p.Ser642Ter
XM_017023672.2:c.1919C>G	XP_016879161.1:p.Ser640Ter
XM_017023673.2:c.1919C>G	XP_016879162.1:p.Ser640Ter
NM_024675.4:c.1919C>G MANE Select	NP_078951.2:p.Ser640Ter