Canonical Allele Identifier: CA395141099

Gene: PALB2

Linked Data

• gnomAD v4: 16-23641127-A-T
• MyVariant Identifiers: chr16:g.23652448A>T (hg19) ; chr16:g.23641127A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641127A>T , CM000678.2:g.23641127A>T	GRCh38
NC_000016.9:g.23652448A>T , CM000678.1:g.23652448A>T	GRCh37
NC_000016.8:g.23559949A>T	NCBI36
NG_007406.1:g.5231T>A , LRG_308:g.5231T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-822T>A	ENSP00000460666.3:n.-822T>A
ENST00000565038.2:c.31T>A	ENSP00000459882.2:p.Cys11Ser
ENST00000566069.6:c.31T>A	ENSP00000459237.2:p.Cys11Ser
ENST00000697377.2:c.-209T>A	ENSP00000513286.2:n.-209T>A
ENST00000697379.2:c.-115T>A	ENSP00000513287.2:n.-115T>A
ENST00000561514.2:c.-1713T>A	ENSP00000460666.2:n.-1713T>A
ENST00000697374.1:c.-1304T>A	ENSP00000513284.1:n.-1304T>A
ENST00000697376.1:c.-1025T>A	ENSP00000513285.1:n.-1025T>A
ENST00000697377.1:c.-1100T>A	ENSP00000513286.1:n.-1100T>A
ENST00000697379.1:c.-1006T>A	ENSP00000513287.1:n.-1006T>A
ENST00000697382.1:c.-1764T>A	ENSP00000513288.1:n.-1764T>A
ENST00000697383.1:c.31T>A	ENSP00000513289.1:p.Cys11Ser
ENST00000697384.1:n.185T>A
ENST00000261584.9:c.31T>A MANE Select	ENSP00000261584.4:p.Cys11Ser
ENST00000261584.8:c.31T>A	ENSP00000261584.4:p.Cys11Ser
ENST00000567003.1:n.175T>A
ENST00000568219.5:c.-838T>A	ENSP00000454703.2:n.-838T>A
NM_024675.3:c.31T>A , LRG_308t1:c.31T>A	NP_078951.2:p.Cys11Ser
XM_011545948.1:c.-989T>A	XP_011544250.1:n.-989T>A
XM_011545946.2:c.-822T>A	XP_011544248.1:n.-822T>A
XM_011545947.2:c.-822T>A	XP_011544249.1:n.-822T>A
XM_011545948.2:c.-989T>A	XP_011544250.1:n.-989T>A
XM_017023671.1:c.-822T>A	XP_016879160.1:n.-822T>A
XM_017023672.2:c.31T>A	XP_016879161.1:p.Cys11Ser
XM_017023673.2:c.31T>A	XP_016879162.1:p.Cys11Ser
NM_024675.4:c.31T>A MANE Select	NP_078951.2:p.Cys11Ser