Canonical Allele Identifier: CA2213412211

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23622987G= , CM000678.2:g.23622987G=	GRCh38
NC_000016.9:g.23634308G= , CM000678.1:g.23634308G=	GRCh37
NC_000016.8:g.23541809G=	NCBI36
NG_007406.1:g.23371C= , LRG_308:g.23371C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.2984C=	ENSP00000460666.3:p.Thr995=
ENST00000565038.2:c.*459C=	ENSP00000459882.2:n.*459C=
ENST00000566069.6:c.2978C=	ENSP00000459237.2:p.Thr993=
ENST00000697377.2:c.2822C=	ENSP00000513286.2:p.Thr941=
ENST00000697379.2:c.2984C=	ENSP00000513287.2:p.Thr995=
ENST00000561514.2:c.2093C=	ENSP00000460666.2:p.Thr698=
ENST00000697374.1:c.2093C=	ENSP00000513284.1:p.Thr698=
ENST00000697375.1:n.4325C=
ENST00000697376.1:c.2093C=	ENSP00000513285.1:p.Thr698=
ENST00000697377.1:c.1931C=	ENSP00000513286.1:p.Thr644=
ENST00000697378.1:n.3498C=
ENST00000697379.1:c.2093C=	ENSP00000513287.1:p.Thr698=
ENST00000697380.1:n.2270C=
ENST00000697381.1:n.1673C=
ENST00000697382.1:c.2093C=	ENSP00000513288.1:p.Thr698=
ENST00000697383.1:c.512C=	ENSP00000513289.1:p.Thr171=
ENST00000261584.9:c.2978C= MANE Select	ENSP00000261584.4:p.Thr993=
ENST00000261584.8:c.2978C=	ENSP00000261584.4:p.Thr993=
ENST00000568219.5:c.2093C=	ENSP00000454703.2:p.Thr698=
NM_024675.3:c.2978C= , LRG_308t1:c.2978C=	NP_078951.2:p.Thr993=
XM_011545946.1:c.2984C=	XP_011544248.1:p.Thr995=
XM_011545947.1:c.2984C=	XP_011544249.1:p.Thr995=
XM_011545948.1:c.2093C=	XP_011544250.1:p.Thr698=
XR_950851.1:n.3774C=
XM_011545946.2:c.2984C=	XP_011544248.1:p.Thr995=
XM_011545947.2:c.2984C=	XP_011544249.1:p.Thr995=
XM_011545948.2:c.2093C=	XP_011544250.1:p.Thr698=
XM_017023671.1:c.2984C=	XP_016879160.1:p.Thr995=
XM_017023672.2:c.2978C=	XP_016879161.1:p.Thr993=
XM_017023673.2:c.2978C=	XP_016879162.1:p.Thr993=
NM_024675.4:c.2978C= MANE Select	NP_078951.2:p.Thr993=