Canonical Allele Identifier: CA395138277

Gene: PALB2

Linked Data

• ClinVar Variation Id: 1483004
• ClinVar RCV Id: RCV002025323
• dbSNP Id: rs1567205179
• MyVariant Identifiers: chr16:g.23614955G>T (hg19) ; chr16:g.23603634G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23603634G>T , CM000678.2:g.23603634G>T	GRCh38
NC_000016.9:g.23614955G>T , CM000678.1:g.23614955G>T	GRCh37
NC_000016.8:g.23522456G>T	NCBI36
NG_007406.1:g.42724C>A , LRG_308:g.42724C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3392C>A	ENSP00000460666.3:p.Ala1131Glu
ENST00000565038.2:c.*871C>A	ENSP00000459882.2:n.*871C>A
ENST00000566069.6:c.*21C>A	ENSP00000459237.2:n.*21C>A
ENST00000697377.2:c.3230C>A	ENSP00000513286.2:p.Ala1077Glu
ENST00000697379.2:c.3392C>A	ENSP00000513287.2:p.Ala1131Glu
ENST00000561514.2:c.2501C>A	ENSP00000460666.2:p.Ala834Glu
ENST00000697374.1:c.2501C>A	ENSP00000513284.1:p.Ala834Glu
ENST00000697375.1:n.4733C>A
ENST00000697376.1:c.*21C>A	ENSP00000513285.1:n.*21C>A
ENST00000697377.1:c.2339C>A	ENSP00000513286.1:p.Ala780Glu
ENST00000697378.1:n.3906C>A
ENST00000697379.1:c.2501C>A	ENSP00000513287.1:p.Ala834Glu
ENST00000697380.1:n.2590C>A
ENST00000697381.1:n.2081C>A
ENST00000697382.1:c.*163C>A	ENSP00000513288.1:n.*163C>A
ENST00000697383.1:c.920C>A	ENSP00000513289.1:p.Ala307Glu
ENST00000261584.9:c.3386C>A MANE Select	ENSP00000261584.4:p.Ala1129Glu
ENST00000261584.8:c.3386C>A	ENSP00000261584.4:p.Ala1129Glu
ENST00000566069.5:c.152C>A
ENST00000568219.5:c.2501C>A	ENSP00000454703.2:p.Ala834Glu
NM_024675.3:c.3386C>A , LRG_308t1:c.3386C>A	NP_078951.2:p.Ala1129Glu
XM_011545946.1:c.3392C>A	XP_011544248.1:p.Ala1131Glu
XM_011545947.1:c.*21C>A	XP_011544249.1:n.*21C>A
XM_011545948.1:c.2501C>A	XP_011544250.1:p.Ala834Glu
XR_950851.1:n.4094C>A
XM_011545946.2:c.3392C>A	XP_011544248.1:p.Ala1131Glu
XM_011545947.2:c.*21C>A	XP_011544249.1:n.*21C>A
XM_011545948.2:c.2501C>A	XP_011544250.1:p.Ala834Glu
XM_017023671.1:c.3155C>A	XP_016879160.1:p.Ala1052Glu
XM_017023672.2:c.3149C>A	XP_016879161.1:p.Ala1050Glu
XM_017023673.2:c.*21C>A	XP_016879162.1:n.*21C>A
NM_024675.4:c.3386C>A MANE Select	NP_078951.2:p.Ala1129Glu