Canonical Allele Identifier: CA395144193

Gene: PALB2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23623045T>C , CM000678.2:g.23623045T>C	GRCh38
NC_000016.9:g.23634366T>C , CM000678.1:g.23634366T>C	GRCh37
NC_000016.8:g.23541867T>C	NCBI36
NG_007406.1:g.23313A>G , LRG_308:g.23313A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2926A>G	ENSP00000460666.3:p.Lys976Glu
ENST00000565038.2:c.*401A>G	ENSP00000459882.2:n.*401A>G
ENST00000566069.6:c.2920A>G	ENSP00000459237.2:p.Lys974Glu
ENST00000697377.2:c.2764A>G	ENSP00000513286.2:p.Lys922Glu
ENST00000697379.2:c.2926A>G	ENSP00000513287.2:p.Lys976Glu
ENST00000561514.2:c.2035A>G	ENSP00000460666.2:p.Lys679Glu
ENST00000697374.1:c.2035A>G	ENSP00000513284.1:p.Lys679Glu
ENST00000697375.1:n.4267A>G
ENST00000697376.1:c.2035A>G	ENSP00000513285.1:p.Lys679Glu
ENST00000697377.1:c.1873A>G	ENSP00000513286.1:p.Lys625Glu
ENST00000697378.1:n.3440A>G
ENST00000697379.1:c.2035A>G	ENSP00000513287.1:p.Lys679Glu
ENST00000697380.1:n.2212A>G
ENST00000697381.1:n.1615A>G
ENST00000697382.1:c.2035A>G	ENSP00000513288.1:p.Lys679Glu
ENST00000697383.1:c.454A>G	ENSP00000513289.1:p.Lys152Glu
ENST00000261584.9:c.2920A>G MANE Select	ENSP00000261584.4:p.Lys974Glu
ENST00000261584.8:c.2920A>G	ENSP00000261584.4:p.Lys974Glu
ENST00000568219.5:c.2035A>G	ENSP00000454703.2:p.Lys679Glu
NM_024675.3:c.2920A>G , LRG_308t1:c.2920A>G	NP_078951.2:p.Lys974Glu
XM_011545946.1:c.2926A>G	XP_011544248.1:p.Lys976Glu
XM_011545947.1:c.2926A>G	XP_011544249.1:p.Lys976Glu
XM_011545948.1:c.2035A>G	XP_011544250.1:p.Lys679Glu
XR_950851.1:n.3716A>G
XM_011545946.2:c.2926A>G	XP_011544248.1:p.Lys976Glu
XM_011545947.2:c.2926A>G	XP_011544249.1:p.Lys976Glu
XM_011545948.2:c.2035A>G	XP_011544250.1:p.Lys679Glu
XM_017023671.1:c.2926A>G	XP_016879160.1:p.Lys976Glu
XM_017023672.2:c.2920A>G	XP_016879161.1:p.Lys974Glu
XM_017023673.2:c.2920A>G	XP_016879162.1:p.Lys974Glu
NM_024675.4:c.2920A>G MANE Select	NP_078951.2:p.Lys974Glu