Canonical Allele Identifier: CA395144366

Gene: PALB2

Linked Data

• ClinVar Variation Id: 1691512
• ClinVar RCV Id: RCV002254841
• dbSNP Id: rs2142337057
• MyVariant Identifiers: chr16:g.23634410A>G (hg19) ; chr16:g.23623089A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23623089A>G , CM000678.2:g.23623089A>G	GRCh38
NC_000016.9:g.23634410A>G , CM000678.1:g.23634410A>G	GRCh37
NC_000016.8:g.23541911A>G	NCBI36
NG_007406.1:g.23269T>C , LRG_308:g.23269T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2882T>C	ENSP00000460666.3:p.Val961Ala
ENST00000565038.2:c.*357T>C	ENSP00000459882.2:n.*357T>C
ENST00000566069.6:c.2876T>C	ENSP00000459237.2:p.Val959Ala
ENST00000697377.2:c.2720T>C	ENSP00000513286.2:p.Val907Ala
ENST00000697379.2:c.2882T>C	ENSP00000513287.2:p.Val961Ala
ENST00000561514.2:c.1991T>C	ENSP00000460666.2:p.Val664Ala
ENST00000697374.1:c.1991T>C	ENSP00000513284.1:p.Val664Ala
ENST00000697375.1:n.4223T>C
ENST00000697376.1:c.1991T>C	ENSP00000513285.1:p.Val664Ala
ENST00000697377.1:c.1829T>C	ENSP00000513286.1:p.Val610Ala
ENST00000697378.1:n.3396T>C
ENST00000697379.1:c.1991T>C	ENSP00000513287.1:p.Val664Ala
ENST00000697380.1:n.2168T>C
ENST00000697381.1:n.1571T>C
ENST00000697382.1:c.1991T>C	ENSP00000513288.1:p.Val664Ala
ENST00000697383.1:c.410T>C	ENSP00000513289.1:p.Val137Ala
ENST00000261584.9:c.2876T>C MANE Select	ENSP00000261584.4:p.Val959Ala
ENST00000261584.8:c.2876T>C	ENSP00000261584.4:p.Val959Ala
ENST00000568219.5:c.1991T>C	ENSP00000454703.2:p.Val664Ala
NM_024675.3:c.2876T>C , LRG_308t1:c.2876T>C	NP_078951.2:p.Val959Ala
XM_011545946.1:c.2882T>C	XP_011544248.1:p.Val961Ala
XM_011545947.1:c.2882T>C	XP_011544249.1:p.Val961Ala
XM_011545948.1:c.1991T>C	XP_011544250.1:p.Val664Ala
XR_950851.1:n.3672T>C
XM_011545946.2:c.2882T>C	XP_011544248.1:p.Val961Ala
XM_011545947.2:c.2882T>C	XP_011544249.1:p.Val961Ala
XM_011545948.2:c.1991T>C	XP_011544250.1:p.Val664Ala
XM_017023671.1:c.2882T>C	XP_016879160.1:p.Val961Ala
XM_017023672.2:c.2876T>C	XP_016879161.1:p.Val959Ala
XM_017023673.2:c.2876T>C	XP_016879162.1:p.Val959Ala
NM_024675.4:c.2876T>C MANE Select	NP_078951.2:p.Val959Ala