Canonical Allele Identifier: CA7963709

Gene: PALB2

Linked Data

• ClinVar Variation Id: 923896
• ClinVar RCV Id: RCV001184920 ; RCV002559881
• dbSNP Id: rs753470554
• ExAC: 16:23646423 G / A
• gnomAD v2: 16-23646423-G-A
• gnomAD v4: 16-23635102-G-A
• COSMIC: COSM4990860
• MyVariant Identifiers: chr16:g.23646423G>A (hg19) ; chr16:g.23635102G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635102G>A , CM000678.2:g.23635102G>A	GRCh38
NC_000016.9:g.23646423G>A , CM000678.1:g.23646423G>A	GRCh37
NC_000016.8:g.23553924G>A	NCBI36
NG_007406.1:g.11256C>T , LRG_308:g.11256C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1450C>T	ENSP00000460666.3:p.Leu484Phe
ENST00000565038.2:c.211+2748C>T	ENSP00000459882.2:n.211+2748C>T
ENST00000566069.6:c.1444C>T	ENSP00000459237.2:p.Leu482Phe
ENST00000697377.2:c.1450C>T	ENSP00000513286.2:p.Leu484Phe
ENST00000697379.2:c.1450C>T	ENSP00000513287.2:p.Leu484Phe
ENST00000561514.2:c.559C>T	ENSP00000460666.2:p.Leu187Phe
ENST00000697374.1:c.559C>T	ENSP00000513284.1:p.Leu187Phe
ENST00000697375.1:n.2791C>T
ENST00000697376.1:c.559C>T	ENSP00000513285.1:p.Leu187Phe
ENST00000697377.1:c.559C>T	ENSP00000513286.1:p.Leu187Phe
ENST00000697378.1:n.1964C>T
ENST00000697379.1:c.559C>T	ENSP00000513287.1:p.Leu187Phe
ENST00000697382.1:c.559C>T	ENSP00000513288.1:p.Leu187Phe
ENST00000697383.1:c.49-5827C>T	ENSP00000513289.1:n.49-5827C>T
ENST00000697384.1:n.1598C>T
ENST00000261584.9:c.1444C>T MANE Select	ENSP00000261584.4:p.Leu482Phe
ENST00000261584.8:c.1444C>T	ENSP00000261584.4:p.Leu482Phe
ENST00000565038.1:c.86+2748C>T
ENST00000568219.5:c.559C>T	ENSP00000454703.2:p.Leu187Phe
NM_024675.3:c.1444C>T , LRG_308t1:c.1444C>T	NP_078951.2:p.Leu482Phe
XM_011545946.1:c.1450C>T	XP_011544248.1:p.Leu484Phe
XM_011545947.1:c.1450C>T	XP_011544249.1:p.Leu484Phe
XM_011545948.1:c.559C>T	XP_011544250.1:p.Leu187Phe
XR_950851.1:n.2240C>T
XM_011545946.2:c.1450C>T	XP_011544248.1:p.Leu484Phe
XM_011545947.2:c.1450C>T	XP_011544249.1:p.Leu484Phe
XM_011545948.2:c.559C>T	XP_011544250.1:p.Leu187Phe
XM_017023671.1:c.1450C>T	XP_016879160.1:p.Leu484Phe
XM_017023672.2:c.1444C>T	XP_016879161.1:p.Leu482Phe
XM_017023673.2:c.1444C>T	XP_016879162.1:p.Leu482Phe
NM_024675.4:c.1444C>T MANE Select	NP_078951.2:p.Leu482Phe