Canonical Allele Identifier: CA395137400

Gene: PALB2

Linked Data

• ClinVar Variation Id: 1737172
• ClinVar RCV Id: RCV002359536
• dbSNP Id: rs1967049086
• MyVariant Identifiers: chr16:g.23647465G>T (hg19) ; chr16:g.23636144G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23636144G>T , CM000678.2:g.23636144G>T	GRCh38
NC_000016.9:g.23647465G>T , CM000678.1:g.23647465G>T	GRCh37
NC_000016.8:g.23554966G>T	NCBI36
NG_007406.1:g.10214C>A , LRG_308:g.10214C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.408C>A	ENSP00000460666.3:p.Asp136Glu
ENST00000565038.2:c.211+1706C>A	ENSP00000459882.2:n.211+1706C>A
ENST00000566069.6:c.402C>A	ENSP00000459237.2:p.Asp134Glu
ENST00000697377.2:c.408C>A	ENSP00000513286.2:p.Asp136Glu
ENST00000697379.2:c.408C>A	ENSP00000513287.2:p.Asp136Glu
ENST00000561514.2:c.-484C>A	ENSP00000460666.2:n.-484C>A
ENST00000697374.1:c.-484C>A	ENSP00000513284.1:n.-484C>A
ENST00000697375.1:n.1749C>A
ENST00000697376.1:c.-484C>A	ENSP00000513285.1:n.-484C>A
ENST00000697377.1:c.-484C>A	ENSP00000513286.1:n.-484C>A
ENST00000697378.1:n.922C>A
ENST00000697379.1:c.-484C>A	ENSP00000513287.1:n.-484C>A
ENST00000697382.1:c.-484C>A	ENSP00000513288.1:n.-484C>A
ENST00000697383.1:c.48+4966C>A	ENSP00000513289.1:n.48+4966C>A
ENST00000697384.1:n.556C>A
ENST00000261584.9:c.402C>A MANE Select	ENSP00000261584.4:p.Asp134Glu
ENST00000261584.8:c.402C>A	ENSP00000261584.4:p.Asp134Glu
ENST00000565038.1:c.86+1706C>A
ENST00000567003.1:n.680C>A
ENST00000568219.5:c.-484C>A	ENSP00000454703.2:n.-484C>A
NM_024675.3:c.402C>A , LRG_308t1:c.402C>A	NP_078951.2:p.Asp134Glu
XM_011545946.1:c.408C>A	XP_011544248.1:p.Asp136Glu
XM_011545947.1:c.408C>A	XP_011544249.1:p.Asp136Glu
XM_011545948.1:c.-484C>A	XP_011544250.1:n.-484C>A
XR_950851.1:n.1198C>A
XM_011545946.2:c.408C>A	XP_011544248.1:p.Asp136Glu
XM_011545947.2:c.408C>A	XP_011544249.1:p.Asp136Glu
XM_011545948.2:c.-484C>A	XP_011544250.1:n.-484C>A
XM_017023671.1:c.408C>A	XP_016879160.1:p.Asp136Glu
XM_017023672.2:c.402C>A	XP_016879161.1:p.Asp134Glu
XM_017023673.2:c.402C>A	XP_016879162.1:p.Asp134Glu
NM_024675.4:c.402C>A MANE Select	NP_078951.2:p.Asp134Glu