Canonical Allele Identifier: CA395130924

Gene: PALB2

Linked Data

• ClinVar Variation Id: 1378403
• ClinVar RCV Id: RCV001881121
• dbSNP Id: rs1966959567
• gnomAD v4: 16-23635012-A-G
• MyVariant Identifiers: chr16:g.23646333A>G (hg19) ; chr16:g.23635012A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635012A>G , CM000678.2:g.23635012A>G	GRCh38
NC_000016.9:g.23646333A>G , CM000678.1:g.23646333A>G	GRCh37
NC_000016.8:g.23553834A>G	NCBI36
NG_007406.1:g.11346T>C , LRG_308:g.11346T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1540T>C	ENSP00000460666.3:p.Tyr514His
ENST00000565038.2:c.211+2838T>C	ENSP00000459882.2:n.211+2838T>C
ENST00000566069.6:c.1534T>C	ENSP00000459237.2:p.Tyr512His
ENST00000697377.2:c.1540T>C	ENSP00000513286.2:p.Tyr514His
ENST00000697379.2:c.1540T>C	ENSP00000513287.2:p.Tyr514His
ENST00000561514.2:c.649T>C	ENSP00000460666.2:p.Tyr217His
ENST00000697374.1:c.649T>C	ENSP00000513284.1:p.Tyr217His
ENST00000697375.1:n.2881T>C
ENST00000697376.1:c.649T>C	ENSP00000513285.1:p.Tyr217His
ENST00000697377.1:c.649T>C	ENSP00000513286.1:p.Tyr217His
ENST00000697378.1:n.2054T>C
ENST00000697379.1:c.649T>C	ENSP00000513287.1:p.Tyr217His
ENST00000697382.1:c.649T>C	ENSP00000513288.1:p.Tyr217His
ENST00000697383.1:c.49-5737T>C	ENSP00000513289.1:n.49-5737T>C
ENST00000697384.1:n.1688T>C
ENST00000261584.9:c.1534T>C MANE Select	ENSP00000261584.4:p.Tyr512His
ENST00000261584.8:c.1534T>C	ENSP00000261584.4:p.Tyr512His
ENST00000565038.1:c.86+2838T>C
ENST00000568219.5:c.649T>C	ENSP00000454703.2:p.Tyr217His
NM_024675.3:c.1534T>C , LRG_308t1:c.1534T>C	NP_078951.2:p.Tyr512His
XM_011545946.1:c.1540T>C	XP_011544248.1:p.Tyr514His
XM_011545947.1:c.1540T>C	XP_011544249.1:p.Tyr514His
XM_011545948.1:c.649T>C	XP_011544250.1:p.Tyr217His
XR_950851.1:n.2330T>C
XM_011545946.2:c.1540T>C	XP_011544248.1:p.Tyr514His
XM_011545947.2:c.1540T>C	XP_011544249.1:p.Tyr514His
XM_011545948.2:c.649T>C	XP_011544250.1:p.Tyr217His
XM_017023671.1:c.1540T>C	XP_016879160.1:p.Tyr514His
XM_017023672.2:c.1534T>C	XP_016879161.1:p.Tyr512His
XM_017023673.2:c.1534T>C	XP_016879162.1:p.Tyr512His
NM_024675.4:c.1534T>C MANE Select	NP_078951.2:p.Tyr512His