Canonical Allele Identifier: CA395141231

Gene: PALB2

Linked Data

• dbSNP Id: rs2142481773
• MyVariant Identifiers: chr16:g.23652471T>A (hg19) ; chr16:g.23641150T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641150T>A , CM000678.2:g.23641150T>A	GRCh38
NC_000016.9:g.23652471T>A , CM000678.1:g.23652471T>A	GRCh37
NC_000016.8:g.23559972T>A	NCBI36
NG_007406.1:g.5208A>T , LRG_308:g.5208A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-845A>T	ENSP00000460666.3:n.-845A>T
ENST00000565038.2:c.8A>T	ENSP00000459882.2:p.Glu3Val
ENST00000566069.6:c.8A>T	ENSP00000459237.2:p.Glu3Val
ENST00000697377.2:c.-232A>T	ENSP00000513286.2:n.-232A>T
ENST00000697379.2:c.-138A>T	ENSP00000513287.2:n.-138A>T
ENST00000561514.2:c.-1736A>T	ENSP00000460666.2:n.-1736A>T
ENST00000697374.1:c.-1327A>T	ENSP00000513284.1:n.-1327A>T
ENST00000697376.1:c.-1048A>T	ENSP00000513285.1:n.-1048A>T
ENST00000697377.1:c.-1123A>T	ENSP00000513286.1:n.-1123A>T
ENST00000697379.1:c.-1029A>T	ENSP00000513287.1:n.-1029A>T
ENST00000697382.1:c.-1787A>T	ENSP00000513288.1:n.-1787A>T
ENST00000697383.1:c.8A>T	ENSP00000513289.1:p.Glu3Val
ENST00000697384.1:n.162A>T
ENST00000261584.9:c.8A>T MANE Select	ENSP00000261584.4:p.Glu3Val
ENST00000261584.8:c.8A>T	ENSP00000261584.4:p.Glu3Val
ENST00000567003.1:n.152A>T
ENST00000568219.5:c.-861A>T	ENSP00000454703.2:n.-861A>T
NM_024675.3:c.8A>T , LRG_308t1:c.8A>T	NP_078951.2:p.Glu3Val
XM_011545948.1:c.-1012A>T	XP_011544250.1:n.-1012A>T
XM_011545946.2:c.-845A>T	XP_011544248.1:n.-845A>T
XM_011545947.2:c.-845A>T	XP_011544249.1:n.-845A>T
XM_011545948.2:c.-1012A>T	XP_011544250.1:n.-1012A>T
XM_017023671.1:c.-845A>T	XP_016879160.1:n.-845A>T
XM_017023672.2:c.8A>T	XP_016879161.1:p.Glu3Val
XM_017023673.2:c.8A>T	XP_016879162.1:p.Glu3Val
NM_024675.4:c.8A>T MANE Select	NP_078951.2:p.Glu3Val