Canonical Allele Identifier: CA395127489

Gene: PALB2

Linked Data

• ClinVar Variation Id: 820357
• ClinVar RCV Id: RCV001013733 ; RCV003607373
• dbSNP Id: rs1597090741
• gnomAD v4: 16-23630228-C-T
• MyVariant Identifiers: chr16:g.23641549C>T (hg19) ; chr16:g.23630228C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23630228C>T , CM000678.2:g.23630228C>T	GRCh38
NC_000016.9:g.23641549C>T , CM000678.1:g.23641549C>T	GRCh37
NC_000016.8:g.23549050C>T	NCBI36
NG_007406.1:g.16130G>A , LRG_308:g.16130G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1932G>A	ENSP00000460666.3:p.Met644Ile
ENST00000565038.2:c.212-953G>A	ENSP00000459882.2:n.212-953G>A
ENST00000566069.6:c.1926G>A	ENSP00000459237.2:p.Met642Ile
ENST00000697377.2:c.1932G>A	ENSP00000513286.2:p.Met644Ile
ENST00000697379.2:c.1932G>A	ENSP00000513287.2:p.Met644Ile
ENST00000561514.2:c.1041G>A	ENSP00000460666.2:p.Met347Ile
ENST00000697374.1:c.1041G>A	ENSP00000513284.1:p.Met347Ile
ENST00000697375.1:n.3273G>A
ENST00000697376.1:c.1041G>A	ENSP00000513285.1:p.Met347Ile
ENST00000697377.1:c.1041G>A	ENSP00000513286.1:p.Met347Ile
ENST00000697378.1:n.2446G>A
ENST00000697379.1:c.1041G>A	ENSP00000513287.1:p.Met347Ile
ENST00000697380.1:n.854G>A
ENST00000697381.1:n.621G>A
ENST00000697382.1:c.1041G>A	ENSP00000513288.1:p.Met347Ile
ENST00000697383.1:c.49-953G>A	ENSP00000513289.1:n.49-953G>A
ENST00000697384.1:n.2080G>A
ENST00000261584.9:c.1926G>A MANE Select	ENSP00000261584.4:p.Met642Ile
ENST00000261584.8:c.1926G>A	ENSP00000261584.4:p.Met642Ile
ENST00000565038.1:c.87-953G>A
ENST00000568219.5:c.1041G>A	ENSP00000454703.2:p.Met347Ile
NM_024675.3:c.1926G>A , LRG_308t1:c.1926G>A	NP_078951.2:p.Met642Ile
XM_011545946.1:c.1932G>A	XP_011544248.1:p.Met644Ile
XM_011545947.1:c.1932G>A	XP_011544249.1:p.Met644Ile
XM_011545948.1:c.1041G>A	XP_011544250.1:p.Met347Ile
XR_950851.1:n.2722G>A
XM_011545946.2:c.1932G>A	XP_011544248.1:p.Met644Ile
XM_011545947.2:c.1932G>A	XP_011544249.1:p.Met644Ile
XM_011545948.2:c.1041G>A	XP_011544250.1:p.Met347Ile
XM_017023671.1:c.1932G>A	XP_016879160.1:p.Met644Ile
XM_017023672.2:c.1926G>A	XP_016879161.1:p.Met642Ile
XM_017023673.2:c.1926G>A	XP_016879162.1:p.Met642Ile
NM_024675.4:c.1926G>A MANE Select	NP_078951.2:p.Met642Ile