Canonical Allele Identifier: CA2695197461

Gene: PALB2

Linked Data

• ClinVar Variation Id: 2673906
• ClinVar RCV Id: RCV003450522

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23629679del , CM000678.2:g.23629679del	GRCh38
NC_000016.9:g.23641000del , CM000678.1:g.23641000del	GRCh37
NC_000016.8:g.23548501del	NCBI36
NG_007406.1:g.16681del , LRG_308:g.16681del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2483del	ENSP00000460666.3:p.Asn828ThrfsTer25
ENST00000565038.2:c.212-402del	ENSP00000459882.2:n.212-402del
ENST00000566069.6:c.2477del	ENSP00000459237.2:p.Asn826ThrfsTer25
ENST00000697377.2:c.2483del	ENSP00000513286.2:p.Asn828ThrfsTer25
ENST00000697379.2:c.2483del	ENSP00000513287.2:p.Asn828ThrfsTer25
ENST00000561514.2:c.1592del	ENSP00000460666.2:p.Asn531ThrfsTer25
ENST00000697374.1:c.1592del	ENSP00000513284.1:p.Asn531ThrfsTer25
ENST00000697375.1:n.3824del
ENST00000697376.1:c.1592del	ENSP00000513285.1:p.Asn531ThrfsTer25
ENST00000697377.1:c.1592del	ENSP00000513286.1:p.Asn531ThrfsTer25
ENST00000697378.1:n.2997del
ENST00000697379.1:c.1592del	ENSP00000513287.1:p.Asn531ThrfsTer25
ENST00000697380.1:n.1405del
ENST00000697381.1:n.1172del
ENST00000697382.1:c.1592del	ENSP00000513288.1:p.Asn531ThrfsTer25
ENST00000697383.1:c.49-402del	ENSP00000513289.1:n.49-402del
ENST00000697384.1:n.2631del
ENST00000261584.9:c.2477del MANE Select	ENSP00000261584.4:p.Asn826ThrfsTer25
ENST00000261584.8:c.2477del	ENSP00000261584.4:p.Asn826ThrfsTer25
ENST00000565038.1:c.87-402del
ENST00000568219.5:c.1592del	ENSP00000454703.2:p.Asn531ThrfsTer25
NM_024675.3:c.2477del , LRG_308t1:c.2477del	NP_078951.2:p.Asn826ThrfsTer25
XM_011545946.1:c.2483del	XP_011544248.1:p.Asn828ThrfsTer25
XM_011545947.1:c.2483del	XP_011544249.1:p.Asn828ThrfsTer25
XM_011545948.1:c.1592del	XP_011544250.1:p.Asn531ThrfsTer25
XR_950851.1:n.3273del
XM_011545946.2:c.2483del	XP_011544248.1:p.Asn828ThrfsTer25
XM_011545947.2:c.2483del	XP_011544249.1:p.Asn828ThrfsTer25
XM_011545948.2:c.1592del	XP_011544250.1:p.Asn531ThrfsTer25
XM_017023671.1:c.2483del	XP_016879160.1:p.Asn828ThrfsTer25
XM_017023672.2:c.2477del	XP_016879161.1:p.Asn826ThrfsTer25
XM_017023673.2:c.2477del	XP_016879162.1:p.Asn826ThrfsTer25
NM_024675.4:c.2477del MANE Select	NP_078951.2:p.Asn826ThrfsTer25