Canonical Allele Identifier: CA395136591

Gene: PALB2

Linked Data

• ClinVar Variation Id: 1362077
• ClinVar RCV Id: RCV001899993 ; RCV002361111
• dbSNP Id: rs878976819
• MyVariant Identifiers: chr16:g.23647239G>T (hg19) ; chr16:g.23635918G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635918G>T , CM000678.2:g.23635918G>T	GRCh38
NC_000016.9:g.23647239G>T , CM000678.1:g.23647239G>T	GRCh37
NC_000016.8:g.23554740G>T	NCBI36
NG_007406.1:g.10440C>A , LRG_308:g.10440C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.634C>A	ENSP00000460666.3:p.Pro212Thr
ENST00000565038.2:c.211+1932C>A	ENSP00000459882.2:n.211+1932C>A
ENST00000566069.6:c.628C>A	ENSP00000459237.2:p.Pro210Thr
ENST00000697377.2:c.634C>A	ENSP00000513286.2:p.Pro212Thr
ENST00000697379.2:c.634C>A	ENSP00000513287.2:p.Pro212Thr
ENST00000561514.2:c.-258C>A	ENSP00000460666.2:n.-258C>A
ENST00000697374.1:c.-258C>A	ENSP00000513284.1:n.-258C>A
ENST00000697375.1:n.1975C>A
ENST00000697376.1:c.-258C>A	ENSP00000513285.1:n.-258C>A
ENST00000697377.1:c.-258C>A	ENSP00000513286.1:n.-258C>A
ENST00000697378.1:n.1148C>A
ENST00000697379.1:c.-258C>A	ENSP00000513287.1:n.-258C>A
ENST00000697382.1:c.-258C>A	ENSP00000513288.1:n.-258C>A
ENST00000697383.1:c.48+5192C>A	ENSP00000513289.1:n.48+5192C>A
ENST00000697384.1:n.782C>A
ENST00000261584.9:c.628C>A MANE Select	ENSP00000261584.4:p.Pro210Thr
ENST00000261584.8:c.628C>A	ENSP00000261584.4:p.Pro210Thr
ENST00000565038.1:c.86+1932C>A
ENST00000568219.5:c.-258C>A	ENSP00000454703.2:n.-258C>A
NM_024675.3:c.628C>A , LRG_308t1:c.628C>A	NP_078951.2:p.Pro210Thr
XM_011545946.1:c.634C>A	XP_011544248.1:p.Pro212Thr
XM_011545947.1:c.634C>A	XP_011544249.1:p.Pro212Thr
XM_011545948.1:c.-258C>A	XP_011544250.1:n.-258C>A
XR_950851.1:n.1424C>A
XM_011545946.2:c.634C>A	XP_011544248.1:p.Pro212Thr
XM_011545947.2:c.634C>A	XP_011544249.1:p.Pro212Thr
XM_011545948.2:c.-258C>A	XP_011544250.1:n.-258C>A
XM_017023671.1:c.634C>A	XP_016879160.1:p.Pro212Thr
XM_017023672.2:c.628C>A	XP_016879161.1:p.Pro210Thr
XM_017023673.2:c.628C>A	XP_016879162.1:p.Pro210Thr
NM_024675.4:c.628C>A MANE Select	NP_078951.2:p.Pro210Thr