Canonical Allele Identifier: CA395127274

Gene: PALB2

Linked Data

• dbSNP Id: rs1597090541
• MyVariant Identifiers: chr16:g.23641495A>C (hg19) ; chr16:g.23630174A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23630174A>C , CM000678.2:g.23630174A>C	GRCh38
NC_000016.9:g.23641495A>C , CM000678.1:g.23641495A>C	GRCh37
NC_000016.8:g.23548996A>C	NCBI36
NG_007406.1:g.16184T>G , LRG_308:g.16184T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1986T>G	ENSP00000460666.3:p.Ser662Arg
ENST00000565038.2:c.212-899T>G	ENSP00000459882.2:n.212-899T>G
ENST00000566069.6:c.1980T>G	ENSP00000459237.2:p.Ser660Arg
ENST00000697377.2:c.1986T>G	ENSP00000513286.2:p.Ser662Arg
ENST00000697379.2:c.1986T>G	ENSP00000513287.2:p.Ser662Arg
ENST00000561514.2:c.1095T>G	ENSP00000460666.2:p.Ser365Arg
ENST00000697374.1:c.1095T>G	ENSP00000513284.1:p.Ser365Arg
ENST00000697375.1:n.3327T>G
ENST00000697376.1:c.1095T>G	ENSP00000513285.1:p.Ser365Arg
ENST00000697377.1:c.1095T>G	ENSP00000513286.1:p.Ser365Arg
ENST00000697378.1:n.2500T>G
ENST00000697379.1:c.1095T>G	ENSP00000513287.1:p.Ser365Arg
ENST00000697380.1:n.908T>G
ENST00000697381.1:n.675T>G
ENST00000697382.1:c.1095T>G	ENSP00000513288.1:p.Ser365Arg
ENST00000697383.1:c.49-899T>G	ENSP00000513289.1:n.49-899T>G
ENST00000697384.1:n.2134T>G
ENST00000261584.9:c.1980T>G MANE Select	ENSP00000261584.4:p.Ser660Arg
ENST00000261584.8:c.1980T>G	ENSP00000261584.4:p.Ser660Arg
ENST00000565038.1:c.87-899T>G
ENST00000568219.5:c.1095T>G	ENSP00000454703.2:p.Ser365Arg
NM_024675.3:c.1980T>G , LRG_308t1:c.1980T>G	NP_078951.2:p.Ser660Arg
XM_011545946.1:c.1986T>G	XP_011544248.1:p.Ser662Arg
XM_011545947.1:c.1986T>G	XP_011544249.1:p.Ser662Arg
XM_011545948.1:c.1095T>G	XP_011544250.1:p.Ser365Arg
XR_950851.1:n.2776T>G
XM_011545946.2:c.1986T>G	XP_011544248.1:p.Ser662Arg
XM_011545947.2:c.1986T>G	XP_011544249.1:p.Ser662Arg
XM_011545948.2:c.1095T>G	XP_011544250.1:p.Ser365Arg
XM_017023671.1:c.1986T>G	XP_016879160.1:p.Ser662Arg
XM_017023672.2:c.1980T>G	XP_016879161.1:p.Ser660Arg
XM_017023673.2:c.1980T>G	XP_016879162.1:p.Ser660Arg
NM_024675.4:c.1980T>G MANE Select	NP_078951.2:p.Ser660Arg