Canonical Allele Identifier: CA395121847

Gene: PALB2

Linked Data

• dbSNP Id: rs1597084930
• MyVariant Identifiers: chr16:g.23637571A>T (hg19) ; chr16:g.23626250A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23626250A>T , CM000678.2:g.23626250A>T	GRCh38
NC_000016.9:g.23637571A>T , CM000678.1:g.23637571A>T	GRCh37
NC_000016.8:g.23545072A>T	NCBI36
NG_007406.1:g.20108T>A , LRG_308:g.20108T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.2740T>A	ENSP00000460666.3:p.Trp914Arg
ENST00000565038.2:c.*215T>A	ENSP00000459882.2:n.*215T>A
ENST00000566069.6:c.2734T>A	ENSP00000459237.2:p.Trp912Arg
ENST00000697377.2:c.2593-2156T>A	ENSP00000513286.2:n.2593-2156T>A
ENST00000697379.2:c.2740T>A	ENSP00000513287.2:p.Trp914Arg
ENST00000561514.2:c.1849T>A	ENSP00000460666.2:p.Trp617Arg
ENST00000697374.1:c.1849T>A	ENSP00000513284.1:p.Trp617Arg
ENST00000697375.1:n.4081T>A
ENST00000697376.1:c.1849T>A	ENSP00000513285.1:p.Trp617Arg
ENST00000697377.1:c.1702-2156T>A	ENSP00000513286.1:n.1702-2156T>A
ENST00000697378.1:n.3254T>A
ENST00000697379.1:c.1849T>A	ENSP00000513287.1:p.Trp617Arg
ENST00000697380.1:n.2026T>A
ENST00000697381.1:n.1429T>A
ENST00000697382.1:c.1849T>A	ENSP00000513288.1:p.Trp617Arg
ENST00000697383.1:c.268T>A	ENSP00000513289.1:p.Trp90Arg
ENST00000261584.9:c.2734T>A MANE Select	ENSP00000261584.4:p.Trp912Arg
ENST00000261584.8:c.2734T>A	ENSP00000261584.4:p.Trp912Arg
ENST00000565038.1:c.306T>A
ENST00000568219.5:c.1849T>A	ENSP00000454703.2:p.Trp617Arg
NM_024675.3:c.2734T>A , LRG_308t1:c.2734T>A	NP_078951.2:p.Trp912Arg
XM_011545946.1:c.2740T>A	XP_011544248.1:p.Trp914Arg
XM_011545947.1:c.2740T>A	XP_011544249.1:p.Trp914Arg
XM_011545948.1:c.1849T>A	XP_011544250.1:p.Trp617Arg
XR_950851.1:n.3530T>A
XM_011545946.2:c.2740T>A	XP_011544248.1:p.Trp914Arg
XM_011545947.2:c.2740T>A	XP_011544249.1:p.Trp914Arg
XM_011545948.2:c.1849T>A	XP_011544250.1:p.Trp617Arg
XM_017023671.1:c.2740T>A	XP_016879160.1:p.Trp914Arg
XM_017023672.2:c.2734T>A	XP_016879161.1:p.Trp912Arg
XM_017023673.2:c.2734T>A	XP_016879162.1:p.Trp912Arg
NM_024675.4:c.2734T>A MANE Select	NP_078951.2:p.Trp912Arg