Canonical Allele Identifier: CA2213431441

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635979T= , CM000678.2:g.23635979T=	GRCh38
NC_000016.9:g.23647300T= , CM000678.1:g.23647300T=	GRCh37
NC_000016.8:g.23554801T=	NCBI36
NG_007406.1:g.10379A= , LRG_308:g.10379A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.573A=	ENSP00000460666.3:p.Arg191=
ENST00000565038.2:c.211+1871A=	ENSP00000459882.2:n.211+1871A=
ENST00000566069.6:c.567A=	ENSP00000459237.2:p.Arg189=
ENST00000697377.2:c.573A=	ENSP00000513286.2:p.Arg191=
ENST00000697379.2:c.573A=	ENSP00000513287.2:p.Arg191=
ENST00000561514.2:c.-319A=	ENSP00000460666.2:n.-319A=
ENST00000697374.1:c.-319A=	ENSP00000513284.1:n.-319A=
ENST00000697375.1:n.1914A=
ENST00000697376.1:c.-319A=	ENSP00000513285.1:n.-319A=
ENST00000697377.1:c.-319A=	ENSP00000513286.1:n.-319A=
ENST00000697378.1:n.1087A=
ENST00000697379.1:c.-319A=	ENSP00000513287.1:n.-319A=
ENST00000697382.1:c.-319A=	ENSP00000513288.1:n.-319A=
ENST00000697383.1:c.48+5131A=	ENSP00000513289.1:n.48+5131A=
ENST00000697384.1:n.721A=
ENST00000261584.9:c.567A= MANE Select	ENSP00000261584.4:p.Arg189=
ENST00000261584.8:c.567A=	ENSP00000261584.4:p.Arg189=
ENST00000565038.1:c.86+1871A=
ENST00000568219.5:c.-319A=	ENSP00000454703.2:n.-319A=
NM_024675.3:c.567A= , LRG_308t1:c.567A=	NP_078951.2:p.Arg189=
XM_011545946.1:c.573A=	XP_011544248.1:p.Arg191=
XM_011545947.1:c.573A=	XP_011544249.1:p.Arg191=
XM_011545948.1:c.-319A=	XP_011544250.1:n.-319A=
XR_950851.1:n.1363A=
XM_011545946.2:c.573A=	XP_011544248.1:p.Arg191=
XM_011545947.2:c.573A=	XP_011544249.1:p.Arg191=
XM_011545948.2:c.-319A=	XP_011544250.1:n.-319A=
XM_017023671.1:c.573A=	XP_016879160.1:p.Arg191=
XM_017023672.2:c.567A=	XP_016879161.1:p.Arg189=
XM_017023673.2:c.567A=	XP_016879162.1:p.Arg189=
NM_024675.4:c.567A= MANE Select	NP_078951.2:p.Arg189=