Canonical Allele Identifier: CA395138031

Gene: PALB2

Linked Data

• dbSNP Id: rs1597062038
• MyVariant Identifiers: chr16:g.23614872G>T (hg19) ; chr16:g.23603551G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23603551G>T , CM000678.2:g.23603551G>T	GRCh38
NC_000016.9:g.23614872G>T , CM000678.1:g.23614872G>T	GRCh37
NC_000016.8:g.23522373G>T	NCBI36
NG_007406.1:g.42807C>A , LRG_308:g.42807C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3475C>A	ENSP00000460666.3:p.Gln1159Lys
ENST00000565038.2:c.*954C>A	ENSP00000459882.2:n.*954C>A
ENST00000566069.6:c.*104C>A	ENSP00000459237.2:n.*104C>A
ENST00000697377.2:c.3313C>A	ENSP00000513286.2:p.Gln1105Lys
ENST00000697379.2:c.3475C>A	ENSP00000513287.2:p.Gln1159Lys
ENST00000561514.2:c.2584C>A	ENSP00000460666.2:p.Gln862Lys
ENST00000697374.1:c.2584C>A	ENSP00000513284.1:p.Gln862Lys
ENST00000697375.1:n.4816C>A
ENST00000697376.1:c.*104C>A	ENSP00000513285.1:n.*104C>A
ENST00000697377.1:c.2422C>A	ENSP00000513286.1:p.Gln808Lys
ENST00000697378.1:n.3989C>A
ENST00000697379.1:c.2584C>A	ENSP00000513287.1:p.Gln862Lys
ENST00000697380.1:n.2673C>A
ENST00000697381.1:n.2164C>A
ENST00000697382.1:c.*246C>A	ENSP00000513288.1:n.*246C>A
ENST00000697383.1:c.1003C>A	ENSP00000513289.1:p.Gln335Lys
ENST00000261584.9:c.3469C>A MANE Select	ENSP00000261584.4:p.Gln1157Lys
ENST00000261584.8:c.3469C>A	ENSP00000261584.4:p.Gln1157Lys
ENST00000566069.5:c.235C>A
ENST00000568219.5:c.2584C>A	ENSP00000454703.2:p.Gln862Lys
NM_024675.3:c.3469C>A , LRG_308t1:c.3469C>A	NP_078951.2:p.Gln1157Lys
XM_011545946.1:c.3475C>A	XP_011544248.1:p.Gln1159Lys
XM_011545947.1:c.*104C>A	XP_011544249.1:n.*104C>A
XM_011545948.1:c.2584C>A	XP_011544250.1:p.Gln862Lys
XR_950851.1:n.4177C>A
XM_011545946.2:c.3475C>A	XP_011544248.1:p.Gln1159Lys
XM_011545947.2:c.*104C>A	XP_011544249.1:n.*104C>A
XM_011545948.2:c.2584C>A	XP_011544250.1:p.Gln862Lys
XM_017023671.1:c.3238C>A	XP_016879160.1:p.Gln1080Lys
XM_017023672.2:c.3232C>A	XP_016879161.1:p.Gln1078Lys
XM_017023673.2:c.*104C>A	XP_016879162.1:n.*104C>A
NM_024675.4:c.3469C>A MANE Select	NP_078951.2:p.Gln1157Lys