Canonical Allele Identifier: CA494461714

Gene: PALB2

Linked Data

• dbSNP Id: rs543266199
• MyVariant Identifiers: chr16:g.23646889T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635568T>A , CM000678.2:g.23635568T>A	GRCh38
NC_000016.9:g.23646889T>A , CM000678.1:g.23646889T>A	GRCh37
NC_000016.8:g.23554390T>A	NCBI36
NG_007406.1:g.10790A>T , LRG_308:g.10790A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.984A>T	ENSP00000460666.3:p.Ser328=
ENST00000565038.2:c.211+2282A>T	ENSP00000459882.2:n.211+2282A>T
ENST00000566069.6:c.978A>T	ENSP00000459237.2:p.Ser326=
ENST00000697377.2:c.984A>T	ENSP00000513286.2:p.Ser328=
ENST00000697379.2:c.984A>T	ENSP00000513287.2:p.Ser328=
ENST00000561514.2:c.93A>T	ENSP00000460666.2:p.Ser31=
ENST00000697374.1:c.93A>T	ENSP00000513284.1:p.Ser31=
ENST00000697375.1:n.2325A>T
ENST00000697376.1:c.93A>T	ENSP00000513285.1:p.Ser31=
ENST00000697377.1:c.93A>T	ENSP00000513286.1:p.Ser31=
ENST00000697378.1:n.1498A>T
ENST00000697379.1:c.93A>T	ENSP00000513287.1:p.Ser31=
ENST00000697382.1:c.93A>T	ENSP00000513288.1:p.Ser31=
ENST00000697383.1:c.48+5542A>T	ENSP00000513289.1:n.48+5542A>T
ENST00000697384.1:n.1132A>T
ENST00000261584.9:c.978A>T MANE Select	ENSP00000261584.4:p.Ser326=
ENST00000261584.8:c.978A>T	ENSP00000261584.4:p.Ser326=
ENST00000565038.1:c.86+2282A>T
ENST00000568219.5:c.93A>T	ENSP00000454703.2:p.Ser31=
NM_024675.3:c.978A>T , LRG_308t1:c.978A>T	NP_078951.2:p.Ser326=
XM_011545946.1:c.984A>T	XP_011544248.1:p.Ser328=
XM_011545947.1:c.984A>T	XP_011544249.1:p.Ser328=
XM_011545948.1:c.93A>T	XP_011544250.1:p.Ser31=
XR_950851.1:n.1774A>T
XM_011545946.2:c.984A>T	XP_011544248.1:p.Ser328=
XM_011545947.2:c.984A>T	XP_011544249.1:p.Ser328=
XM_011545948.2:c.93A>T	XP_011544250.1:p.Ser31=
XM_017023671.1:c.984A>T	XP_016879160.1:p.Ser328=
XM_017023672.2:c.978A>T	XP_016879161.1:p.Ser326=
XM_017023673.2:c.978A>T	XP_016879162.1:p.Ser326=
NM_024675.4:c.978A>T MANE Select	NP_078951.2:p.Ser326=