Canonical Allele Identifier: CA2213428817

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635281T= , CM000678.2:g.23635281T=	GRCh38
NC_000016.9:g.23646602T= , CM000678.1:g.23646602T=	GRCh37
NC_000016.8:g.23554103T=	NCBI36
NG_007406.1:g.11077A= , LRG_308:g.11077A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1271A=	ENSP00000460666.3:p.Lys424=
ENST00000565038.2:c.211+2569A=	ENSP00000459882.2:n.211+2569A=
ENST00000566069.6:c.1265A=	ENSP00000459237.2:p.Lys422=
ENST00000697377.2:c.1271A=	ENSP00000513286.2:p.Lys424=
ENST00000697379.2:c.1271A=	ENSP00000513287.2:p.Lys424=
ENST00000561514.2:c.380A=	ENSP00000460666.2:p.Lys127=
ENST00000697374.1:c.380A=	ENSP00000513284.1:p.Lys127=
ENST00000697375.1:n.2612A=
ENST00000697376.1:c.380A=	ENSP00000513285.1:p.Lys127=
ENST00000697377.1:c.380A=	ENSP00000513286.1:p.Lys127=
ENST00000697378.1:n.1785A=
ENST00000697379.1:c.380A=	ENSP00000513287.1:p.Lys127=
ENST00000697382.1:c.380A=	ENSP00000513288.1:p.Lys127=
ENST00000697383.1:c.48+5829A=	ENSP00000513289.1:n.48+5829A=
ENST00000697384.1:n.1419A=
ENST00000261584.9:c.1265A= MANE Select	ENSP00000261584.4:p.Lys422=
ENST00000261584.8:c.1265A=	ENSP00000261584.4:p.Lys422=
ENST00000565038.1:c.86+2569A=
ENST00000568219.5:c.380A=	ENSP00000454703.2:p.Lys127=
NM_024675.3:c.1265A= , LRG_308t1:c.1265A=	NP_078951.2:p.Lys422=
XM_011545946.1:c.1271A=	XP_011544248.1:p.Lys424=
XM_011545947.1:c.1271A=	XP_011544249.1:p.Lys424=
XM_011545948.1:c.380A=	XP_011544250.1:p.Lys127=
XR_950851.1:n.2061A=
XM_011545946.2:c.1271A=	XP_011544248.1:p.Lys424=
XM_011545947.2:c.1271A=	XP_011544249.1:p.Lys424=
XM_011545948.2:c.380A=	XP_011544250.1:p.Lys127=
XM_017023671.1:c.1271A=	XP_016879160.1:p.Lys424=
XM_017023672.2:c.1265A=	XP_016879161.1:p.Lys422=
XM_017023673.2:c.1265A=	XP_016879162.1:p.Lys422=
NM_024675.4:c.1265A= MANE Select	NP_078951.2:p.Lys422=