Canonical Allele Identifier: CA395141088

Gene: PALB2

Linked Data

• MyVariant Identifiers: chr16:g.23652447C>G (hg19) ; chr16:g.23641126C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641126C>G , CM000678.2:g.23641126C>G	GRCh38
NC_000016.9:g.23652447C>G , CM000678.1:g.23652447C>G	GRCh37
NC_000016.8:g.23559948C>G	NCBI36
NG_007406.1:g.5232G>C , LRG_308:g.5232G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-821G>C	ENSP00000460666.3:n.-821G>C
ENST00000565038.2:c.32G>C	ENSP00000459882.2:p.Cys11Ser
ENST00000566069.6:c.32G>C	ENSP00000459237.2:p.Cys11Ser
ENST00000697377.2:c.-208G>C	ENSP00000513286.2:n.-208G>C
ENST00000697379.2:c.-114G>C	ENSP00000513287.2:n.-114G>C
ENST00000561514.2:c.-1712G>C	ENSP00000460666.2:n.-1712G>C
ENST00000697374.1:c.-1303G>C	ENSP00000513284.1:n.-1303G>C
ENST00000697376.1:c.-1024G>C	ENSP00000513285.1:n.-1024G>C
ENST00000697377.1:c.-1099G>C	ENSP00000513286.1:n.-1099G>C
ENST00000697379.1:c.-1005G>C	ENSP00000513287.1:n.-1005G>C
ENST00000697382.1:c.-1763G>C	ENSP00000513288.1:n.-1763G>C
ENST00000697383.1:c.32G>C	ENSP00000513289.1:p.Cys11Ser
ENST00000697384.1:n.186G>C
ENST00000261584.9:c.32G>C MANE Select	ENSP00000261584.4:p.Cys11Ser
ENST00000261584.8:c.32G>C	ENSP00000261584.4:p.Cys11Ser
ENST00000567003.1:n.176G>C
ENST00000568219.5:c.-838+1G>C	ENSP00000454703.2:n.-838+1G>C
NM_024675.3:c.32G>C , LRG_308t1:c.32G>C	NP_078951.2:p.Cys11Ser
XM_011545948.1:c.-988G>C	XP_011544250.1:n.-988G>C
XM_011545946.2:c.-821G>C	XP_011544248.1:n.-821G>C
XM_011545947.2:c.-821G>C	XP_011544249.1:n.-821G>C
XM_011545948.2:c.-988G>C	XP_011544250.1:n.-988G>C
XM_017023671.1:c.-821G>C	XP_016879160.1:n.-821G>C
XM_017023672.2:c.32G>C	XP_016879161.1:p.Cys11Ser
XM_017023673.2:c.32G>C	XP_016879162.1:p.Cys11Ser
NM_024675.4:c.32G>C MANE Select	NP_078951.2:p.Cys11Ser