Canonical Allele Identifier: CA2213436456

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641154C= , CM000678.2:g.23641154C=	GRCh38
NC_000016.9:g.23652475C= , CM000678.1:g.23652475C=	GRCh37
NC_000016.8:g.23559976C=	NCBI36
NG_007406.1:g.5204G= , LRG_308:g.5204G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.-849G=	ENSP00000460666.3:n.-849G=
ENST00000565038.2:c.4G=	ENSP00000459882.2:p.Asp2=
ENST00000566069.6:c.4G=	ENSP00000459237.2:p.Asp2=
ENST00000697377.2:c.-236G=	ENSP00000513286.2:n.-236G=
ENST00000697379.2:c.-142G=	ENSP00000513287.2:n.-142G=
ENST00000561514.2:c.-1740G=	ENSP00000460666.2:n.-1740G=
ENST00000697374.1:c.-1331G=	ENSP00000513284.1:n.-1331G=
ENST00000697376.1:c.-1052G=	ENSP00000513285.1:n.-1052G=
ENST00000697377.1:c.-1127G=	ENSP00000513286.1:n.-1127G=
ENST00000697379.1:c.-1033G=	ENSP00000513287.1:n.-1033G=
ENST00000697382.1:c.-1791G=	ENSP00000513288.1:n.-1791G=
ENST00000697383.1:c.4G=	ENSP00000513289.1:p.Asp2=
ENST00000697384.1:n.158G=
ENST00000261584.9:c.4G= MANE Select	ENSP00000261584.4:p.Asp2=
ENST00000261584.8:c.4G=	ENSP00000261584.4:p.Asp2=
ENST00000567003.1:n.148G=
ENST00000568219.5:c.-865G=	ENSP00000454703.2:n.-865G=
NM_024675.3:c.4G= , LRG_308t1:c.4G=	NP_078951.2:p.Asp2=
XM_011545948.1:c.-1016G=	XP_011544250.1:n.-1016G=
XM_011545946.2:c.-849G=	XP_011544248.1:n.-849G=
XM_011545947.2:c.-849G=	XP_011544249.1:n.-849G=
XM_011545948.2:c.-1016G=	XP_011544250.1:n.-1016G=
XM_017023671.1:c.-849G=	XP_016879160.1:n.-849G=
XM_017023672.2:c.4G=	XP_016879161.1:p.Asp2=
XM_017023673.2:c.4G=	XP_016879162.1:p.Asp2=
NM_024675.4:c.4G= MANE Select	NP_078951.2:p.Asp2=