Canonical Allele Identifier: CA2213436431

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641128G= , CM000678.2:g.23641128G=	GRCh38
NC_000016.9:g.23652449G= , CM000678.1:g.23652449G=	GRCh37
NC_000016.8:g.23559950G=	NCBI36
NG_007406.1:g.5230C= , LRG_308:g.5230C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-823C=	ENSP00000460666.3:n.-823C=
ENST00000565038.2:c.30C=	ENSP00000459882.2:p.Ser10=
ENST00000566069.6:c.30C=	ENSP00000459237.2:p.Ser10=
ENST00000697377.2:c.-210C=	ENSP00000513286.2:n.-210C=
ENST00000697379.2:c.-116C=	ENSP00000513287.2:n.-116C=
ENST00000561514.2:c.-1714C=	ENSP00000460666.2:n.-1714C=
ENST00000697374.1:c.-1305C=	ENSP00000513284.1:n.-1305C=
ENST00000697376.1:c.-1026C=	ENSP00000513285.1:n.-1026C=
ENST00000697377.1:c.-1101C=	ENSP00000513286.1:n.-1101C=
ENST00000697379.1:c.-1007C=	ENSP00000513287.1:n.-1007C=
ENST00000697382.1:c.-1765C=	ENSP00000513288.1:n.-1765C=
ENST00000697383.1:c.30C=	ENSP00000513289.1:p.Ser10=
ENST00000697384.1:n.184C=
ENST00000261584.9:c.30C= MANE Select	ENSP00000261584.4:p.Ser10=
ENST00000261584.8:c.30C=	ENSP00000261584.4:p.Ser10=
ENST00000567003.1:n.174C=
ENST00000568219.5:c.-839C=	ENSP00000454703.2:n.-839C=
NM_024675.3:c.30C= , LRG_308t1:c.30C=	NP_078951.2:p.Ser10=
XM_011545948.1:c.-990C=	XP_011544250.1:n.-990C=
XM_011545946.2:c.-823C=	XP_011544248.1:n.-823C=
XM_011545947.2:c.-823C=	XP_011544249.1:n.-823C=
XM_011545948.2:c.-990C=	XP_011544250.1:n.-990C=
XM_017023671.1:c.-823C=	XP_016879160.1:n.-823C=
XM_017023672.2:c.30C=	XP_016879161.1:p.Ser10=
XM_017023673.2:c.30C=	XP_016879162.1:p.Ser10=
NM_024675.4:c.30C= MANE Select	NP_078951.2:p.Ser10=