Canonical Allele Identifier: CA395144113

Gene: PALB2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23623025G>C , CM000678.2:g.23623025G>C	GRCh38
NC_000016.9:g.23634346G>C , CM000678.1:g.23634346G>C	GRCh37
NC_000016.8:g.23541847G>C	NCBI36
NG_007406.1:g.23333C>G , LRG_308:g.23333C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2946C>G	ENSP00000460666.3:p.Ser982Arg
ENST00000565038.2:c.*421C>G	ENSP00000459882.2:n.*421C>G
ENST00000566069.6:c.2940C>G	ENSP00000459237.2:p.Ser980Arg
ENST00000697377.2:c.2784C>G	ENSP00000513286.2:p.Ser928Arg
ENST00000697379.2:c.2946C>G	ENSP00000513287.2:p.Ser982Arg
ENST00000561514.2:c.2055C>G	ENSP00000460666.2:p.Ser685Arg
ENST00000697374.1:c.2055C>G	ENSP00000513284.1:p.Ser685Arg
ENST00000697375.1:n.4287C>G
ENST00000697376.1:c.2055C>G	ENSP00000513285.1:p.Ser685Arg
ENST00000697377.1:c.1893C>G	ENSP00000513286.1:p.Ser631Arg
ENST00000697378.1:n.3460C>G
ENST00000697379.1:c.2055C>G	ENSP00000513287.1:p.Ser685Arg
ENST00000697380.1:n.2232C>G
ENST00000697381.1:n.1635C>G
ENST00000697382.1:c.2055C>G	ENSP00000513288.1:p.Ser685Arg
ENST00000697383.1:c.474C>G	ENSP00000513289.1:p.Ser158Arg
ENST00000261584.9:c.2940C>G MANE Select	ENSP00000261584.4:p.Ser980Arg
ENST00000261584.8:c.2940C>G	ENSP00000261584.4:p.Ser980Arg
ENST00000568219.5:c.2055C>G	ENSP00000454703.2:p.Ser685Arg
NM_024675.3:c.2940C>G , LRG_308t1:c.2940C>G	NP_078951.2:p.Ser980Arg
XM_011545946.1:c.2946C>G	XP_011544248.1:p.Ser982Arg
XM_011545947.1:c.2946C>G	XP_011544249.1:p.Ser982Arg
XM_011545948.1:c.2055C>G	XP_011544250.1:p.Ser685Arg
XR_950851.1:n.3736C>G
XM_011545946.2:c.2946C>G	XP_011544248.1:p.Ser982Arg
XM_011545947.2:c.2946C>G	XP_011544249.1:p.Ser982Arg
XM_011545948.2:c.2055C>G	XP_011544250.1:p.Ser685Arg
XM_017023671.1:c.2946C>G	XP_016879160.1:p.Ser982Arg
XM_017023672.2:c.2940C>G	XP_016879161.1:p.Ser980Arg
XM_017023673.2:c.2940C>G	XP_016879162.1:p.Ser980Arg
NM_024675.4:c.2940C>G MANE Select	NP_078951.2:p.Ser980Arg