Canonical Allele Identifier: CA10588615

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23637883G>A , CM000678.2:g.23637883G>A	GRCh38
NC_000016.9:g.23649204G>A , CM000678.1:g.23649204G>A	GRCh37
NC_000016.8:g.23556705G>A	NCBI36
NG_007406.1:g.8475C>T , LRG_308:g.8475C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.184C>T	ENSP00000460666.3:p.Gln62Ter
ENST00000565038.2:c.178C>T	ENSP00000459882.2:p.Gln60Ter
ENST00000566069.6:c.178C>T	ENSP00000459237.2:p.Gln60Ter
ENST00000697377.2:c.184C>T	ENSP00000513286.2:p.Gln62Ter
ENST00000697379.2:c.184C>T	ENSP00000513287.2:p.Gln62Ter
ENST00000561514.2:c.-708C>T	ENSP00000460666.2:n.-708C>T
ENST00000697374.1:c.-708C>T	ENSP00000513284.1:n.-708C>T
ENST00000697375.1:n.1525C>T
ENST00000697376.1:c.-708C>T	ENSP00000513285.1:n.-708C>T
ENST00000697377.1:c.-708C>T	ENSP00000513286.1:n.-708C>T
ENST00000697378.1:n.698C>T
ENST00000697379.1:c.-708C>T	ENSP00000513287.1:n.-708C>T
ENST00000697382.1:c.-708C>T	ENSP00000513288.1:n.-708C>T
ENST00000697383.1:c.48+3227C>T	ENSP00000513289.1:n.48+3227C>T
ENST00000697384.1:n.332C>T
ENST00000261584.9:c.178C>T MANE Select	ENSP00000261584.4:p.Gln60Ter
ENST00000261584.8:c.178C>T	ENSP00000261584.4:p.Gln60Ter
ENST00000561514.1:c.184C>T	ENSP00000460666.1:p.Gln62Ter
ENST00000565038.1:c.53C>T
ENST00000567003.1:n.456C>T
ENST00000568219.5:c.-708C>T	ENSP00000454703.2:n.-708C>T
NM_024675.3:c.178C>T , LRG_308t1:c.178C>T	NP_078951.2:p.Gln60Ter
XM_011545946.1:c.184C>T	XP_011544248.1:p.Gln62Ter
XM_011545947.1:c.184C>T	XP_011544249.1:p.Gln62Ter
XM_011545948.1:c.-708C>T	XP_011544250.1:n.-708C>T
XR_950851.1:n.974C>T
XM_011545946.2:c.184C>T	XP_011544248.1:p.Gln62Ter
XM_011545947.2:c.184C>T	XP_011544249.1:p.Gln62Ter
XM_011545948.2:c.-708C>T	XP_011544250.1:n.-708C>T
XM_017023671.1:c.184C>T	XP_016879160.1:p.Gln62Ter
XM_017023672.2:c.178C>T	XP_016879161.1:p.Gln60Ter
XM_017023673.2:c.178C>T	XP_016879162.1:p.Gln60Ter
NM_024675.4:c.178C>T MANE Select	NP_078951.2:p.Gln60Ter