Canonical Allele Identifier: CA269501

Gene: PALB2

Linked Data

• ClinVar Variation Id: 126612
• ClinVar RCV Id: RCV001030243 ; RCV002399478
• dbSNP Id: rs180177104
• MyVariant Identifiers: chr16:g.23646211C>T (hg19) ; chr16:g.23634890C>T (hg38)
• PubMed: PMID:18446436

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23634890C>T , CM000678.2:g.23634890C>T	GRCh38
NC_000016.9:g.23646211C>T , CM000678.1:g.23646211C>T	GRCh37
NC_000016.8:g.23553712C>T	NCBI36
NG_007406.1:g.11468G>A , LRG_308:g.11468G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1662G>A	ENSP00000460666.3:p.Gln554=
ENST00000565038.2:c.211+2960G>A	ENSP00000459882.2:n.211+2960G>A
ENST00000566069.6:c.1656G>A	ENSP00000459237.2:p.Gln552=
ENST00000697377.2:c.1662G>A	ENSP00000513286.2:p.Gln554=
ENST00000697379.2:c.1662G>A	ENSP00000513287.2:p.Gln554=
ENST00000561514.2:c.771G>A	ENSP00000460666.2:p.Gln257=
ENST00000697374.1:c.771G>A	ENSP00000513284.1:p.Gln257=
ENST00000697375.1:n.3003G>A
ENST00000697376.1:c.771G>A	ENSP00000513285.1:p.Gln257=
ENST00000697377.1:c.771G>A	ENSP00000513286.1:p.Gln257=
ENST00000697378.1:n.2176G>A
ENST00000697379.1:c.771G>A	ENSP00000513287.1:p.Gln257=
ENST00000697382.1:c.771G>A	ENSP00000513288.1:p.Gln257=
ENST00000697383.1:c.49-5615G>A	ENSP00000513289.1:n.49-5615G>A
ENST00000697384.1:n.1810G>A
ENST00000261584.9:c.1656G>A MANE Select	ENSP00000261584.4:p.Gln552=
ENST00000261584.8:c.1656G>A	ENSP00000261584.4:p.Gln552=
ENST00000565038.1:c.86+2960G>A
ENST00000568219.5:c.771G>A	ENSP00000454703.2:p.Gln257=
NM_024675.3:c.1656G>A , LRG_308t1:c.1656G>A	NP_078951.2:p.Gln552=
XM_011545946.1:c.1662G>A	XP_011544248.1:p.Gln554=
XM_011545947.1:c.1662G>A	XP_011544249.1:p.Gln554=
XM_011545948.1:c.771G>A	XP_011544250.1:p.Gln257=
XR_950851.1:n.2452G>A
XM_011545946.2:c.1662G>A	XP_011544248.1:p.Gln554=
XM_011545947.2:c.1662G>A	XP_011544249.1:p.Gln554=
XM_011545948.2:c.771G>A	XP_011544250.1:p.Gln257=
XM_017023671.1:c.1662G>A	XP_016879160.1:p.Gln554=
XM_017023672.2:c.1656G>A	XP_016879161.1:p.Gln552=
XM_017023673.2:c.1656G>A	XP_016879162.1:p.Gln552=
NM_024675.4:c.1656G>A MANE Select	NP_078951.2:p.Gln552=