Canonical Allele Identifier: CA395141255

Gene: PALB2

Linked Data

• dbSNP Id: rs1379618411
• MyVariant Identifiers: chr16:g.23652474T>G (hg19) ; chr16:g.23641153T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641153T>G , CM000678.2:g.23641153T>G	GRCh38
NC_000016.9:g.23652474T>G , CM000678.1:g.23652474T>G	GRCh37
NC_000016.8:g.23559975T>G	NCBI36
NG_007406.1:g.5205A>C , LRG_308:g.5205A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-848A>C	ENSP00000460666.3:n.-848A>C
ENST00000565038.2:c.5A>C	ENSP00000459882.2:p.Asp2Ala
ENST00000566069.6:c.5A>C	ENSP00000459237.2:p.Asp2Ala
ENST00000697377.2:c.-235A>C	ENSP00000513286.2:n.-235A>C
ENST00000697379.2:c.-141A>C	ENSP00000513287.2:n.-141A>C
ENST00000561514.2:c.-1739A>C	ENSP00000460666.2:n.-1739A>C
ENST00000697374.1:c.-1330A>C	ENSP00000513284.1:n.-1330A>C
ENST00000697376.1:c.-1051A>C	ENSP00000513285.1:n.-1051A>C
ENST00000697377.1:c.-1126A>C	ENSP00000513286.1:n.-1126A>C
ENST00000697379.1:c.-1032A>C	ENSP00000513287.1:n.-1032A>C
ENST00000697382.1:c.-1790A>C	ENSP00000513288.1:n.-1790A>C
ENST00000697383.1:c.5A>C	ENSP00000513289.1:p.Asp2Ala
ENST00000697384.1:n.159A>C
ENST00000261584.9:c.5A>C MANE Select	ENSP00000261584.4:p.Asp2Ala
ENST00000261584.8:c.5A>C	ENSP00000261584.4:p.Asp2Ala
ENST00000567003.1:n.149A>C
ENST00000568219.5:c.-864A>C	ENSP00000454703.2:n.-864A>C
NM_024675.3:c.5A>C , LRG_308t1:c.5A>C	NP_078951.2:p.Asp2Ala
XM_011545948.1:c.-1015A>C	XP_011544250.1:n.-1015A>C
XM_011545946.2:c.-848A>C	XP_011544248.1:n.-848A>C
XM_011545947.2:c.-848A>C	XP_011544249.1:n.-848A>C
XM_011545948.2:c.-1015A>C	XP_011544250.1:n.-1015A>C
XM_017023671.1:c.-848A>C	XP_016879160.1:n.-848A>C
XM_017023672.2:c.5A>C	XP_016879161.1:p.Asp2Ala
XM_017023673.2:c.5A>C	XP_016879162.1:p.Asp2Ala
NM_024675.4:c.5A>C MANE Select	NP_078951.2:p.Asp2Ala