Canonical Allele Identifier: CA2213436426

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641122C= , CM000678.2:g.23641122C=	GRCh38
NC_000016.9:g.23652443C= , CM000678.1:g.23652443C=	GRCh37
NC_000016.8:g.23559944C=	NCBI36
NG_007406.1:g.5236G= , LRG_308:g.5236G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-817G=	ENSP00000460666.3:n.-817G=
ENST00000565038.2:c.36G=	ENSP00000459882.2:p.Glu12=
ENST00000566069.6:c.36G=	ENSP00000459237.2:p.Glu12=
ENST00000697377.2:c.-204G=	ENSP00000513286.2:n.-204G=
ENST00000697379.2:c.-110G=	ENSP00000513287.2:n.-110G=
ENST00000561514.2:c.-1708G=	ENSP00000460666.2:n.-1708G=
ENST00000697374.1:c.-1299G=	ENSP00000513284.1:n.-1299G=
ENST00000697376.1:c.-1020G=	ENSP00000513285.1:n.-1020G=
ENST00000697377.1:c.-1095G=	ENSP00000513286.1:n.-1095G=
ENST00000697379.1:c.-1001G=	ENSP00000513287.1:n.-1001G=
ENST00000697382.1:c.-1759G=	ENSP00000513288.1:n.-1759G=
ENST00000697383.1:c.36G=	ENSP00000513289.1:p.Glu12=
ENST00000697384.1:n.190G=
ENST00000261584.9:c.36G= MANE Select	ENSP00000261584.4:p.Glu12=
ENST00000261584.8:c.36G=	ENSP00000261584.4:p.Glu12=
ENST00000567003.1:n.180G=
ENST00000568219.5:c.-838+5G=	ENSP00000454703.2:n.-838+5G=
NM_024675.3:c.36G= , LRG_308t1:c.36G=	NP_078951.2:p.Glu12=
XM_011545948.1:c.-984G=	XP_011544250.1:n.-984G=
XM_011545946.2:c.-817G=	XP_011544248.1:n.-817G=
XM_011545947.2:c.-817G=	XP_011544249.1:n.-817G=
XM_011545948.2:c.-984G=	XP_011544250.1:n.-984G=
XM_017023671.1:c.-817G=	XP_016879160.1:n.-817G=
XM_017023672.2:c.36G=	XP_016879161.1:p.Glu12=
XM_017023673.2:c.36G=	XP_016879162.1:p.Glu12=
NM_024675.4:c.36G= MANE Select	NP_078951.2:p.Glu12=