Canonical Allele Identifier: CA395122061

Gene: PALB2

Linked Data

• ClinVar Variation Id: 486011
• ClinVar RCV Id: RCV001350668 ; RCV000573129
• dbSNP Id: rs1555459971
• gnomAD v4: 16-23626316-C-T
• MyVariant Identifiers: chr16:g.23637637C>T (hg19) ; chr16:g.23626316C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23626316C>T , CM000678.2:g.23626316C>T	GRCh38
NC_000016.9:g.23637637C>T , CM000678.1:g.23637637C>T	GRCh37
NC_000016.8:g.23545138C>T	NCBI36
NG_007406.1:g.20042G>A , LRG_308:g.20042G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2674G>A	ENSP00000460666.3:p.Ala892Thr
ENST00000565038.2:c.*149G>A	ENSP00000459882.2:n.*149G>A
ENST00000566069.6:c.2668G>A	ENSP00000459237.2:p.Ala890Thr
ENST00000697377.2:c.2593-2222G>A	ENSP00000513286.2:n.2593-2222G>A
ENST00000697379.2:c.2674G>A	ENSP00000513287.2:p.Ala892Thr
ENST00000561514.2:c.1783G>A	ENSP00000460666.2:p.Ala595Thr
ENST00000697374.1:c.1783G>A	ENSP00000513284.1:p.Ala595Thr
ENST00000697375.1:n.4015G>A
ENST00000697376.1:c.1783G>A	ENSP00000513285.1:p.Ala595Thr
ENST00000697377.1:c.1702-2222G>A	ENSP00000513286.1:n.1702-2222G>A
ENST00000697378.1:n.3188G>A
ENST00000697379.1:c.1783G>A	ENSP00000513287.1:p.Ala595Thr
ENST00000697380.1:n.1960G>A
ENST00000697381.1:n.1363G>A
ENST00000697382.1:c.1783G>A	ENSP00000513288.1:p.Ala595Thr
ENST00000697383.1:c.202G>A	ENSP00000513289.1:p.Ala68Thr
ENST00000261584.9:c.2668G>A MANE Select	ENSP00000261584.4:p.Ala890Thr
ENST00000261584.8:c.2668G>A	ENSP00000261584.4:p.Ala890Thr
ENST00000565038.1:c.240G>A
ENST00000568219.5:c.1783G>A	ENSP00000454703.2:p.Ala595Thr
NM_024675.3:c.2668G>A , LRG_308t1:c.2668G>A	NP_078951.2:p.Ala890Thr
XM_011545946.1:c.2674G>A	XP_011544248.1:p.Ala892Thr
XM_011545947.1:c.2674G>A	XP_011544249.1:p.Ala892Thr
XM_011545948.1:c.1783G>A	XP_011544250.1:p.Ala595Thr
XR_950851.1:n.3464G>A
XM_011545946.2:c.2674G>A	XP_011544248.1:p.Ala892Thr
XM_011545947.2:c.2674G>A	XP_011544249.1:p.Ala892Thr
XM_011545948.2:c.1783G>A	XP_011544250.1:p.Ala595Thr
XM_017023671.1:c.2674G>A	XP_016879160.1:p.Ala892Thr
XM_017023672.2:c.2668G>A	XP_016879161.1:p.Ala890Thr
XM_017023673.2:c.2668G>A	XP_016879162.1:p.Ala890Thr
NM_024675.4:c.2668G>A MANE Select	NP_078951.2:p.Ala890Thr