Canonical Allele Identifier: CA10579970

Gene: PALB2

Linked Data

• ClinVar Variation Id: 232620
• ClinVar RCV Id: RCV000215749 ; RCV000635843 ; RCV002247661
• dbSNP Id: rs876659879
• gnomAD v4: 16-23629706-G-C
• MyVariant Identifiers: chr16:g.23641027G>C (hg19) ; chr16:g.23629706G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23629706G>C , CM000678.2:g.23629706G>C	GRCh38
NC_000016.9:g.23641027G>C , CM000678.1:g.23641027G>C	GRCh37
NC_000016.8:g.23548528G>C	NCBI36
NG_007406.1:g.16652C>G , LRG_308:g.16652C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2454C>G	ENSP00000460666.3:p.Phe818Leu
ENST00000565038.2:c.212-431C>G	ENSP00000459882.2:n.212-431C>G
ENST00000566069.6:c.2448C>G	ENSP00000459237.2:p.Phe816Leu
ENST00000697377.2:c.2454C>G	ENSP00000513286.2:p.Phe818Leu
ENST00000697379.2:c.2454C>G	ENSP00000513287.2:p.Phe818Leu
ENST00000561514.2:c.1563C>G	ENSP00000460666.2:p.Phe521Leu
ENST00000697374.1:c.1563C>G	ENSP00000513284.1:p.Phe521Leu
ENST00000697375.1:n.3795C>G
ENST00000697376.1:c.1563C>G	ENSP00000513285.1:p.Phe521Leu
ENST00000697377.1:c.1563C>G	ENSP00000513286.1:p.Phe521Leu
ENST00000697378.1:n.2968C>G
ENST00000697379.1:c.1563C>G	ENSP00000513287.1:p.Phe521Leu
ENST00000697380.1:n.1376C>G
ENST00000697381.1:n.1143C>G
ENST00000697382.1:c.1563C>G	ENSP00000513288.1:p.Phe521Leu
ENST00000697383.1:c.49-431C>G	ENSP00000513289.1:n.49-431C>G
ENST00000697384.1:n.2602C>G
ENST00000261584.9:c.2448C>G MANE Select	ENSP00000261584.4:p.Phe816Leu
ENST00000261584.8:c.2448C>G	ENSP00000261584.4:p.Phe816Leu
ENST00000565038.1:c.87-431C>G
ENST00000568219.5:c.1563C>G	ENSP00000454703.2:p.Phe521Leu
NM_024675.3:c.2448C>G , LRG_308t1:c.2448C>G	NP_078951.2:p.Phe816Leu
XM_011545946.1:c.2454C>G	XP_011544248.1:p.Phe818Leu
XM_011545947.1:c.2454C>G	XP_011544249.1:p.Phe818Leu
XM_011545948.1:c.1563C>G	XP_011544250.1:p.Phe521Leu
XR_950851.1:n.3244C>G
XM_011545946.2:c.2454C>G	XP_011544248.1:p.Phe818Leu
XM_011545947.2:c.2454C>G	XP_011544249.1:p.Phe818Leu
XM_011545948.2:c.1563C>G	XP_011544250.1:p.Phe521Leu
XM_017023671.1:c.2454C>G	XP_016879160.1:p.Phe818Leu
XM_017023672.2:c.2448C>G	XP_016879161.1:p.Phe816Leu
XM_017023673.2:c.2448C>G	XP_016879162.1:p.Phe816Leu
NM_024675.4:c.2448C>G MANE Select	NP_078951.2:p.Phe816Leu