Canonical Allele Identifier: CA2213424380

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23603545A= , CM000678.2:g.23603545A=	GRCh38
NC_000016.9:g.23614866A= , CM000678.1:g.23614866A=	GRCh37
NC_000016.8:g.23522367A=	NCBI36
NG_007406.1:g.42813T= , LRG_308:g.42813T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3481T=	ENSP00000460666.3:p.Trp1161=
ENST00000565038.2:c.*960T=	ENSP00000459882.2:n.*960T=
ENST00000566069.6:c.*110T=	ENSP00000459237.2:n.*110T=
ENST00000697377.2:c.3319T=	ENSP00000513286.2:p.Trp1107=
ENST00000697379.2:c.3481T=	ENSP00000513287.2:p.Trp1161=
ENST00000561514.2:c.2590T=	ENSP00000460666.2:p.Trp864=
ENST00000697374.1:c.2590T=	ENSP00000513284.1:p.Trp864=
ENST00000697375.1:n.4822T=
ENST00000697376.1:c.*110T=	ENSP00000513285.1:n.*110T=
ENST00000697377.1:c.2428T=	ENSP00000513286.1:p.Trp810=
ENST00000697378.1:n.3995T=
ENST00000697379.1:c.2590T=	ENSP00000513287.1:p.Trp864=
ENST00000697380.1:n.2679T=
ENST00000697381.1:n.2170T=
ENST00000697382.1:c.*252T=	ENSP00000513288.1:n.*252T=
ENST00000697383.1:c.1009T=	ENSP00000513289.1:p.Trp337=
ENST00000261584.9:c.3475T= MANE Select	ENSP00000261584.4:p.Trp1159=
ENST00000261584.8:c.3475T=	ENSP00000261584.4:p.Trp1159=
ENST00000566069.5:c.241T=
ENST00000568219.5:c.2590T=	ENSP00000454703.2:p.Trp864=
NM_024675.3:c.3475T= , LRG_308t1:c.3475T=	NP_078951.2:p.Trp1159=
XM_011545946.1:c.3481T=	XP_011544248.1:p.Trp1161=
XM_011545947.1:c.*110T=	XP_011544249.1:n.*110T=
XM_011545948.1:c.2590T=	XP_011544250.1:p.Trp864=
XR_950851.1:n.4183T=
XM_011545946.2:c.3481T=	XP_011544248.1:p.Trp1161=
XM_011545947.2:c.*110T=	XP_011544249.1:n.*110T=
XM_011545948.2:c.2590T=	XP_011544250.1:p.Trp864=
XM_017023671.1:c.3244T=	XP_016879160.1:p.Trp1082=
XM_017023672.2:c.3238T=	XP_016879161.1:p.Trp1080=
XM_017023673.2:c.*110T=	XP_016879162.1:n.*110T=
NM_024675.4:c.3475T= MANE Select	NP_078951.2:p.Trp1159=