Canonical Allele Identifier: CA2213424295

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23603484T= , CM000678.2:g.23603484T=	GRCh38
NC_000016.9:g.23614805T= , CM000678.1:g.23614805T=	GRCh37
NC_000016.8:g.23522306T=	NCBI36
NG_007406.1:g.42874A= , LRG_308:g.42874A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3542A=	ENSP00000460666.3:p.Asn1181=
ENST00000565038.2:c.*1021A=	ENSP00000459882.2:n.*1021A=
ENST00000566069.6:c.*171A=	ENSP00000459237.2:n.*171A=
ENST00000697377.2:c.3380A=	ENSP00000513286.2:p.Asn1127=
ENST00000697379.2:c.3542A=	ENSP00000513287.2:p.Asn1181=
ENST00000561514.2:c.2651A=	ENSP00000460666.2:p.Asn884=
ENST00000697374.1:c.2651A=	ENSP00000513284.1:p.Asn884=
ENST00000697375.1:n.4883A=
ENST00000697376.1:c.*171A=	ENSP00000513285.1:n.*171A=
ENST00000697377.1:c.2489A=	ENSP00000513286.1:p.Asn830=
ENST00000697378.1:n.4056A=
ENST00000697379.1:c.2651A=	ENSP00000513287.1:p.Asn884=
ENST00000697380.1:n.2740A=
ENST00000697381.1:n.2231A=
ENST00000697382.1:c.*313A=	ENSP00000513288.1:n.*313A=
ENST00000697383.1:c.1070A=	ENSP00000513289.1:p.Asn357=
ENST00000261584.9:c.3536A= MANE Select	ENSP00000261584.4:p.Asn1179=
ENST00000261584.8:c.3536A=	ENSP00000261584.4:p.Asn1179=
ENST00000566069.5:c.302A=
ENST00000568219.5:c.2651A=	ENSP00000454703.2:p.Asn884=
NM_024675.3:c.3536A= , LRG_308t1:c.3536A=	NP_078951.2:p.Asn1179=
XM_011545946.1:c.3542A=	XP_011544248.1:p.Asn1181=
XM_011545947.1:c.*171A=	XP_011544249.1:n.*171A=
XM_011545948.1:c.2651A=	XP_011544250.1:p.Asn884=
XR_950851.1:n.4244A=
XM_011545946.2:c.3542A=	XP_011544248.1:p.Asn1181=
XM_011545947.2:c.*171A=	XP_011544249.1:n.*171A=
XM_011545948.2:c.2651A=	XP_011544250.1:p.Asn884=
XM_017023671.1:c.3305A=	XP_016879160.1:p.Asn1102=
XM_017023672.2:c.3299A=	XP_016879161.1:p.Asn1100=
XM_017023673.2:c.*171A=	XP_016879162.1:n.*171A=
NM_024675.4:c.3536A= MANE Select	NP_078951.2:p.Asn1179=