Canonical Allele Identifier: CA395137806

Gene: PALB2

Linked Data

• ClinVar Variation Id: 2162818
• ClinVar RCV Id: RCV003091471
• dbSNP Id: rs1597099556
• MyVariant Identifiers: chr16:g.23647536C>G (hg19) ; chr16:g.23636215C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23636215C>G , CM000678.2:g.23636215C>G	GRCh38
NC_000016.9:g.23647536C>G , CM000678.1:g.23647536C>G	GRCh37
NC_000016.8:g.23555037C>G	NCBI36
NG_007406.1:g.10143G>C , LRG_308:g.10143G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.337G>C	ENSP00000460666.3:p.Asp113His
ENST00000565038.2:c.211+1635G>C	ENSP00000459882.2:n.211+1635G>C
ENST00000566069.6:c.331G>C	ENSP00000459237.2:p.Asp111His
ENST00000697377.2:c.337G>C	ENSP00000513286.2:p.Asp113His
ENST00000697379.2:c.337G>C	ENSP00000513287.2:p.Asp113His
ENST00000561514.2:c.-555G>C	ENSP00000460666.2:n.-555G>C
ENST00000697374.1:c.-555G>C	ENSP00000513284.1:n.-555G>C
ENST00000697375.1:n.1678G>C
ENST00000697376.1:c.-555G>C	ENSP00000513285.1:n.-555G>C
ENST00000697377.1:c.-555G>C	ENSP00000513286.1:n.-555G>C
ENST00000697378.1:n.851G>C
ENST00000697379.1:c.-555G>C	ENSP00000513287.1:n.-555G>C
ENST00000697382.1:c.-555G>C	ENSP00000513288.1:n.-555G>C
ENST00000697383.1:c.48+4895G>C	ENSP00000513289.1:n.48+4895G>C
ENST00000697384.1:n.485G>C
ENST00000261584.9:c.331G>C MANE Select	ENSP00000261584.4:p.Asp111His
ENST00000261584.8:c.331G>C	ENSP00000261584.4:p.Asp111His
ENST00000565038.1:c.86+1635G>C
ENST00000567003.1:n.609G>C
ENST00000568219.5:c.-555G>C	ENSP00000454703.2:n.-555G>C
NM_024675.3:c.331G>C , LRG_308t1:c.331G>C	NP_078951.2:p.Asp111His
XM_011545946.1:c.337G>C	XP_011544248.1:p.Asp113His
XM_011545947.1:c.337G>C	XP_011544249.1:p.Asp113His
XM_011545948.1:c.-555G>C	XP_011544250.1:n.-555G>C
XR_950851.1:n.1127G>C
XM_011545946.2:c.337G>C	XP_011544248.1:p.Asp113His
XM_011545947.2:c.337G>C	XP_011544249.1:p.Asp113His
XM_011545948.2:c.-555G>C	XP_011544250.1:n.-555G>C
XM_017023671.1:c.337G>C	XP_016879160.1:p.Asp113His
XM_017023672.2:c.331G>C	XP_016879161.1:p.Asp111His
XM_017023673.2:c.331G>C	XP_016879162.1:p.Asp111His
NM_024675.4:c.331G>C MANE Select	NP_078951.2:p.Asp111His