Canonical Allele Identifier: CA2213428806

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23607914A= , CM000678.2:g.23607914A=	GRCh38
NC_000016.9:g.23619235A= , CM000678.1:g.23619235A=	GRCh37
NC_000016.8:g.23526736A=	NCBI36
NG_007406.1:g.38444T= , LRG_308:g.38444T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3306T=	ENSP00000460666.3:p.Thr1102=
ENST00000565038.2:c.*781T=	ENSP00000459882.2:n.*781T=
ENST00000566069.6:c.3202-4245T=	ENSP00000459237.2:n.3202-4245T=
ENST00000697377.2:c.3144T=	ENSP00000513286.2:p.Thr1048=
ENST00000697379.2:c.3306T=	ENSP00000513287.2:p.Thr1102=
ENST00000561514.2:c.2415T=	ENSP00000460666.2:p.Thr805=
ENST00000697374.1:c.2415T=	ENSP00000513284.1:p.Thr805=
ENST00000697375.1:n.4647T=
ENST00000697376.1:c.2317-4245T=	ENSP00000513285.1:n.2317-4245T=
ENST00000697377.1:c.2253T=	ENSP00000513286.1:p.Thr751=
ENST00000697378.1:n.3820T=
ENST00000697379.1:c.2415T=	ENSP00000513287.1:p.Thr805=
ENST00000697380.1:n.2504T=
ENST00000697381.1:n.1995T=
ENST00000697382.1:c.*77T=	ENSP00000513288.1:n.*77T=
ENST00000697383.1:c.834T=	ENSP00000513289.1:p.Thr278=
ENST00000261584.9:c.3300T= MANE Select	ENSP00000261584.4:p.Thr1100=
ENST00000261584.8:c.3300T=	ENSP00000261584.4:p.Thr1100=
ENST00000566069.5:c.117-4245T=
ENST00000568219.5:c.2415T=	ENSP00000454703.2:p.Thr805=
NM_024675.3:c.3300T= , LRG_308t1:c.3300T=	NP_078951.2:p.Thr1100=
XM_011545946.1:c.3306T=	XP_011544248.1:p.Thr1102=
XM_011545947.1:c.3208-4245T=	XP_011544249.1:n.3208-4245T=
XM_011545948.1:c.2415T=	XP_011544250.1:p.Thr805=
XR_950851.1:n.4008T=
XM_011545946.2:c.3306T=	XP_011544248.1:p.Thr1102=
XM_011545947.2:c.3208-4245T=	XP_011544249.1:n.3208-4245T=
XM_011545948.2:c.2415T=	XP_011544250.1:p.Thr805=
XM_017023671.1:c.3120-4245T=	XP_016879160.1:n.3120-4245T=
XM_017023672.2:c.3114-4245T=	XP_016879161.1:n.3114-4245T=
XM_017023673.2:c.3202-4245T=	XP_016879162.1:n.3202-4245T=
NM_024675.4:c.3300T= MANE Select	NP_078951.2:p.Thr1100=