Canonical Allele Identifier: CA494181322

Gene: PALB2

Linked Data

• ClinVar Variation Id: 2020355
• ClinVar RCV Id: RCV002857216
• MyVariant Identifiers: chr16:g.23635420A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23624099A>C , CM000678.2:g.23624099A>C	GRCh38
NC_000016.9:g.23635420A>C , CM000678.1:g.23635420A>C	GRCh37
NC_000016.8:g.23542921A>C	NCBI36
NG_007406.1:g.22259T>G , LRG_308:g.22259T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2755-5T>G	ENSP00000460666.3:n.2755-5T>G
ENST00000565038.2:c.*230-5T>G	ENSP00000459882.2:n.*230-5T>G
ENST00000566069.6:c.2749-5T>G	ENSP00000459237.2:n.2749-5T>G
ENST00000697377.2:c.2593-5T>G	ENSP00000513286.2:n.2593-5T>G
ENST00000697379.2:c.2755-5T>G	ENSP00000513287.2:n.2755-5T>G
ENST00000561514.2:c.1864-5T>G	ENSP00000460666.2:n.1864-5T>G
ENST00000697374.1:c.1864-5T>G	ENSP00000513284.1:n.1864-5T>G
ENST00000697375.1:n.4096-5T>G
ENST00000697376.1:c.1864-5T>G	ENSP00000513285.1:n.1864-5T>G
ENST00000697377.1:c.1702-5T>G	ENSP00000513286.1:n.1702-5T>G
ENST00000697378.1:n.3269-5T>G
ENST00000697379.1:c.1864-5T>G	ENSP00000513287.1:n.1864-5T>G
ENST00000697380.1:n.2041-5T>G
ENST00000697381.1:n.1444-5T>G
ENST00000697382.1:c.1864-5T>G	ENSP00000513288.1:n.1864-5T>G
ENST00000697383.1:c.283-5T>G	ENSP00000513289.1:n.283-5T>G
ENST00000261584.9:c.2749-5T>G MANE Select	ENSP00000261584.4:n.2749-5T>G
ENST00000261584.8:c.2749-5T>G	ENSP00000261584.4:n.2749-5T>G
ENST00000565038.1:c.321-5T>G
ENST00000568219.5:c.1864-5T>G	ENSP00000454703.2:n.1864-5T>G
NM_024675.3:c.2749-5T>G , LRG_308t1:c.2749-5T>G	NP_078951.2:n.2749-5T>G
XM_011545946.1:c.2755-5T>G	XP_011544248.1:n.2755-5T>G
XM_011545947.1:c.2755-5T>G	XP_011544249.1:n.2755-5T>G
XM_011545948.1:c.1864-5T>G	XP_011544250.1:n.1864-5T>G
XR_950851.1:n.3545-5T>G
XM_011545946.2:c.2755-5T>G	XP_011544248.1:n.2755-5T>G
XM_011545947.2:c.2755-5T>G	XP_011544249.1:n.2755-5T>G
XM_011545948.2:c.1864-5T>G	XP_011544250.1:n.1864-5T>G
XM_017023671.1:c.2755-5T>G	XP_016879160.1:n.2755-5T>G
XM_017023672.2:c.2749-5T>G	XP_016879161.1:n.2749-5T>G
XM_017023673.2:c.2749-5T>G	XP_016879162.1:n.2749-5T>G
NM_024675.4:c.2749-5T>G MANE Select	NP_078951.2:n.2749-5T>G