Canonical Allele Identifier: CA10579960

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23626356A>C , CM000678.2:g.23626356A>C	GRCh38
NC_000016.9:g.23637677A>C , CM000678.1:g.23637677A>C	GRCh37
NC_000016.8:g.23545178A>C	NCBI36
NG_007406.1:g.20002T>G , LRG_308:g.20002T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024675.4:c.2628T>G MANE Select	NP_078951.2:p.Phe876Leu
ENST00000261584.9:c.2628T>G MANE Select	ENSP00000261584.4:p.Phe876Leu
NM_024675.3:c.2628T>G , LRG_308t1:c.2628T>G	NP_078951.2:p.Phe876Leu
ENST00000261584.8:c.2628T>G	ENSP00000261584.4:p.Phe876Leu
ENST00000561514.2:c.1743T>G	ENSP00000460666.2:p.Phe581Leu
ENST00000561514.3:c.2634T>G	ENSP00000460666.3:p.Phe878Leu
ENST00000565038.1:c.200T>G
ENST00000565038.2:c.*109T>G	ENSP00000459882.2:n.*109T>G
ENST00000566069.6:c.2628T>G	ENSP00000459237.2:p.Phe876Leu
ENST00000568219.5:c.1743T>G	ENSP00000454703.2:p.Phe581Leu
ENST00000697374.1:c.1743T>G	ENSP00000513284.1:p.Phe581Leu
ENST00000697375.1:n.3975T>G
ENST00000697376.1:c.1743T>G	ENSP00000513285.1:p.Phe581Leu
ENST00000697377.1:c.1702-2262T>G	ENSP00000513286.1:n.1702-2262T>G
ENST00000697377.2:c.2593-2262T>G	ENSP00000513286.2:n.2593-2262T>G
ENST00000697378.1:n.3148T>G
ENST00000697379.1:c.1743T>G	ENSP00000513287.1:p.Phe581Leu
ENST00000697379.2:c.2634T>G	ENSP00000513287.2:p.Phe878Leu
ENST00000697380.1:n.1920T>G
ENST00000697381.1:n.1323T>G
ENST00000697382.1:c.1743T>G	ENSP00000513288.1:p.Phe581Leu
ENST00000697383.1:c.162T>G	ENSP00000513289.1:p.Phe54Leu
XM_011545946.1:c.2634T>G	XP_011544248.1:p.Phe878Leu
XM_011545946.2:c.2634T>G	XP_011544248.1:p.Phe878Leu
XM_011545947.1:c.2634T>G	XP_011544249.1:p.Phe878Leu
XM_011545947.2:c.2634T>G	XP_011544249.1:p.Phe878Leu
XM_011545948.1:c.1743T>G	XP_011544250.1:p.Phe581Leu
XM_011545948.2:c.1743T>G	XP_011544250.1:p.Phe581Leu
XM_017023671.1:c.2634T>G	XP_016879160.1:p.Phe878Leu
XM_017023672.2:c.2628T>G	XP_016879161.1:p.Phe876Leu
XM_017023673.2:c.2628T>G	XP_016879162.1:p.Phe876Leu
XR_950851.1:n.3424T>G