Canonical Allele Identifier: CA395144129

Gene: PALB2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23623027T>C , CM000678.2:g.23623027T>C	GRCh38
NC_000016.9:g.23634348T>C , CM000678.1:g.23634348T>C	GRCh37
NC_000016.8:g.23541849T>C	NCBI36
NG_007406.1:g.23331A>G , LRG_308:g.23331A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2944A>G	ENSP00000460666.3:p.Ser982Gly
ENST00000565038.2:c.*419A>G	ENSP00000459882.2:n.*419A>G
ENST00000566069.6:c.2938A>G	ENSP00000459237.2:p.Ser980Gly
ENST00000697377.2:c.2782A>G	ENSP00000513286.2:p.Ser928Gly
ENST00000697379.2:c.2944A>G	ENSP00000513287.2:p.Ser982Gly
ENST00000561514.2:c.2053A>G	ENSP00000460666.2:p.Ser685Gly
ENST00000697374.1:c.2053A>G	ENSP00000513284.1:p.Ser685Gly
ENST00000697375.1:n.4285A>G
ENST00000697376.1:c.2053A>G	ENSP00000513285.1:p.Ser685Gly
ENST00000697377.1:c.1891A>G	ENSP00000513286.1:p.Ser631Gly
ENST00000697378.1:n.3458A>G
ENST00000697379.1:c.2053A>G	ENSP00000513287.1:p.Ser685Gly
ENST00000697380.1:n.2230A>G
ENST00000697381.1:n.1633A>G
ENST00000697382.1:c.2053A>G	ENSP00000513288.1:p.Ser685Gly
ENST00000697383.1:c.472A>G	ENSP00000513289.1:p.Ser158Gly
ENST00000261584.9:c.2938A>G MANE Select	ENSP00000261584.4:p.Ser980Gly
ENST00000261584.8:c.2938A>G	ENSP00000261584.4:p.Ser980Gly
ENST00000568219.5:c.2053A>G	ENSP00000454703.2:p.Ser685Gly
NM_024675.3:c.2938A>G , LRG_308t1:c.2938A>G	NP_078951.2:p.Ser980Gly
XM_011545946.1:c.2944A>G	XP_011544248.1:p.Ser982Gly
XM_011545947.1:c.2944A>G	XP_011544249.1:p.Ser982Gly
XM_011545948.1:c.2053A>G	XP_011544250.1:p.Ser685Gly
XR_950851.1:n.3734A>G
XM_011545946.2:c.2944A>G	XP_011544248.1:p.Ser982Gly
XM_011545947.2:c.2944A>G	XP_011544249.1:p.Ser982Gly
XM_011545948.2:c.2053A>G	XP_011544250.1:p.Ser685Gly
XM_017023671.1:c.2944A>G	XP_016879160.1:p.Ser982Gly
XM_017023672.2:c.2938A>G	XP_016879161.1:p.Ser980Gly
XM_017023673.2:c.2938A>G	XP_016879162.1:p.Ser980Gly
NM_024675.4:c.2938A>G MANE Select	NP_078951.2:p.Ser980Gly