Canonical Allele Identifier: CA2213431419

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635969T= , CM000678.2:g.23635969T=	GRCh38
NC_000016.9:g.23647290T= , CM000678.1:g.23647290T=	GRCh37
NC_000016.8:g.23554791T=	NCBI36
NG_007406.1:g.10389A= , LRG_308:g.10389A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.583A=	ENSP00000460666.3:p.Thr195=
ENST00000565038.2:c.211+1881A=	ENSP00000459882.2:n.211+1881A=
ENST00000566069.6:c.577A=	ENSP00000459237.2:p.Thr193=
ENST00000697377.2:c.583A=	ENSP00000513286.2:p.Thr195=
ENST00000697379.2:c.583A=	ENSP00000513287.2:p.Thr195=
ENST00000561514.2:c.-309A=	ENSP00000460666.2:n.-309A=
ENST00000697374.1:c.-309A=	ENSP00000513284.1:n.-309A=
ENST00000697375.1:n.1924A=
ENST00000697376.1:c.-309A=	ENSP00000513285.1:n.-309A=
ENST00000697377.1:c.-309A=	ENSP00000513286.1:n.-309A=
ENST00000697378.1:n.1097A=
ENST00000697379.1:c.-309A=	ENSP00000513287.1:n.-309A=
ENST00000697382.1:c.-309A=	ENSP00000513288.1:n.-309A=
ENST00000697383.1:c.48+5141A=	ENSP00000513289.1:n.48+5141A=
ENST00000697384.1:n.731A=
ENST00000261584.9:c.577A= MANE Select	ENSP00000261584.4:p.Thr193=
ENST00000261584.8:c.577A=	ENSP00000261584.4:p.Thr193=
ENST00000565038.1:c.86+1881A=
ENST00000568219.5:c.-309A=	ENSP00000454703.2:n.-309A=
NM_024675.3:c.577A= , LRG_308t1:c.577A=	NP_078951.2:p.Thr193=
XM_011545946.1:c.583A=	XP_011544248.1:p.Thr195=
XM_011545947.1:c.583A=	XP_011544249.1:p.Thr195=
XM_011545948.1:c.-309A=	XP_011544250.1:n.-309A=
XR_950851.1:n.1373A=
XM_011545946.2:c.583A=	XP_011544248.1:p.Thr195=
XM_011545947.2:c.583A=	XP_011544249.1:p.Thr195=
XM_011545948.2:c.-309A=	XP_011544250.1:n.-309A=
XM_017023671.1:c.583A=	XP_016879160.1:p.Thr195=
XM_017023672.2:c.577A=	XP_016879161.1:p.Thr193=
XM_017023673.2:c.577A=	XP_016879162.1:p.Thr193=
NM_024675.4:c.577A= MANE Select	NP_078951.2:p.Thr193=