Canonical Allele Identifier: CA16615240

Gene: PALB2

Linked Data

• ClinVar Variation Id: 410128
• ClinVar RCV Id: RCV000457054 ; RCV001813781
• dbSNP Id: rs1060502748
• MyVariant Identifiers: chr16:g.23641100G>C (hg19) ; chr16:g.23629779G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23629779G>C , CM000678.2:g.23629779G>C	GRCh38
NC_000016.9:g.23641100G>C , CM000678.1:g.23641100G>C	GRCh37
NC_000016.8:g.23548601G>C	NCBI36
NG_007406.1:g.16579C>G , LRG_308:g.16579C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2381C>G	ENSP00000460666.3:p.Ser794Ter
ENST00000565038.2:c.212-504C>G	ENSP00000459882.2:n.212-504C>G
ENST00000566069.6:c.2375C>G	ENSP00000459237.2:p.Ser792Ter
ENST00000697377.2:c.2381C>G	ENSP00000513286.2:p.Ser794Ter
ENST00000697379.2:c.2381C>G	ENSP00000513287.2:p.Ser794Ter
ENST00000561514.2:c.1490C>G	ENSP00000460666.2:p.Ser497Ter
ENST00000697374.1:c.1490C>G	ENSP00000513284.1:p.Ser497Ter
ENST00000697375.1:n.3722C>G
ENST00000697376.1:c.1490C>G	ENSP00000513285.1:p.Ser497Ter
ENST00000697377.1:c.1490C>G	ENSP00000513286.1:p.Ser497Ter
ENST00000697378.1:n.2895C>G
ENST00000697379.1:c.1490C>G	ENSP00000513287.1:p.Ser497Ter
ENST00000697380.1:n.1303C>G
ENST00000697381.1:n.1070C>G
ENST00000697382.1:c.1490C>G	ENSP00000513288.1:p.Ser497Ter
ENST00000697383.1:c.49-504C>G	ENSP00000513289.1:n.49-504C>G
ENST00000697384.1:n.2529C>G
ENST00000261584.9:c.2375C>G MANE Select	ENSP00000261584.4:p.Ser792Ter
ENST00000261584.8:c.2375C>G	ENSP00000261584.4:p.Ser792Ter
ENST00000565038.1:c.87-504C>G
ENST00000568219.5:c.1490C>G	ENSP00000454703.2:p.Ser497Ter
NM_024675.3:c.2375C>G , LRG_308t1:c.2375C>G	NP_078951.2:p.Ser792Ter
XM_011545946.1:c.2381C>G	XP_011544248.1:p.Ser794Ter
XM_011545947.1:c.2381C>G	XP_011544249.1:p.Ser794Ter
XM_011545948.1:c.1490C>G	XP_011544250.1:p.Ser497Ter
XR_950851.1:n.3171C>G
XM_011545946.2:c.2381C>G	XP_011544248.1:p.Ser794Ter
XM_011545947.2:c.2381C>G	XP_011544249.1:p.Ser794Ter
XM_011545948.2:c.1490C>G	XP_011544250.1:p.Ser497Ter
XM_017023671.1:c.2381C>G	XP_016879160.1:p.Ser794Ter
XM_017023672.2:c.2375C>G	XP_016879161.1:p.Ser792Ter
XM_017023673.2:c.2375C>G	XP_016879162.1:p.Ser792Ter
NM_024675.4:c.2375C>G MANE Select	NP_078951.2:p.Ser792Ter