Canonical Allele Identifier: CA395127779

Gene: PALB2

Linked Data

• ClinVar Variation Id: 830148
• ClinVar RCV Id: RCV001030264
• dbSNP Id: rs1966864901
• MyVariant Identifiers: chr16:g.23641622T>A (hg19) ; chr16:g.23630301T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23630301T>A , CM000678.2:g.23630301T>A	GRCh38
NC_000016.9:g.23641622T>A , CM000678.1:g.23641622T>A	GRCh37
NC_000016.8:g.23549123T>A	NCBI36
NG_007406.1:g.16057A>T , LRG_308:g.16057A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1859A>T	ENSP00000460666.3:p.Asp620Val
ENST00000565038.2:c.212-1026A>T	ENSP00000459882.2:n.212-1026A>T
ENST00000566069.6:c.1853A>T	ENSP00000459237.2:p.Asp618Val
ENST00000697377.2:c.1859A>T	ENSP00000513286.2:p.Asp620Val
ENST00000697379.2:c.1859A>T	ENSP00000513287.2:p.Asp620Val
ENST00000561514.2:c.968A>T	ENSP00000460666.2:p.Asp323Val
ENST00000697374.1:c.968A>T	ENSP00000513284.1:p.Asp323Val
ENST00000697375.1:n.3200A>T
ENST00000697376.1:c.968A>T	ENSP00000513285.1:p.Asp323Val
ENST00000697377.1:c.968A>T	ENSP00000513286.1:p.Asp323Val
ENST00000697378.1:n.2373A>T
ENST00000697379.1:c.968A>T	ENSP00000513287.1:p.Asp323Val
ENST00000697380.1:n.781A>T
ENST00000697381.1:n.548A>T
ENST00000697382.1:c.968A>T	ENSP00000513288.1:p.Asp323Val
ENST00000697383.1:c.49-1026A>T	ENSP00000513289.1:n.49-1026A>T
ENST00000697384.1:n.2007A>T
ENST00000261584.9:c.1853A>T MANE Select	ENSP00000261584.4:p.Asp618Val
ENST00000261584.8:c.1853A>T	ENSP00000261584.4:p.Asp618Val
ENST00000565038.1:c.87-1026A>T
ENST00000568219.5:c.968A>T	ENSP00000454703.2:p.Asp323Val
NM_024675.3:c.1853A>T , LRG_308t1:c.1853A>T	NP_078951.2:p.Asp618Val
XM_011545946.1:c.1859A>T	XP_011544248.1:p.Asp620Val
XM_011545947.1:c.1859A>T	XP_011544249.1:p.Asp620Val
XM_011545948.1:c.968A>T	XP_011544250.1:p.Asp323Val
XR_950851.1:n.2649A>T
XM_011545946.2:c.1859A>T	XP_011544248.1:p.Asp620Val
XM_011545947.2:c.1859A>T	XP_011544249.1:p.Asp620Val
XM_011545948.2:c.968A>T	XP_011544250.1:p.Asp323Val
XM_017023671.1:c.1859A>T	XP_016879160.1:p.Asp620Val
XM_017023672.2:c.1853A>T	XP_016879161.1:p.Asp618Val
XM_017023673.2:c.1853A>T	XP_016879162.1:p.Asp618Val
NM_024675.4:c.1853A>T MANE Select	NP_078951.2:p.Asp618Val