Canonical Allele Identifier: CA2213409901

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23621406T= , CM000678.2:g.23621406T=	GRCh38
NC_000016.9:g.23632727T= , CM000678.1:g.23632727T=	GRCh37
NC_000016.8:g.23540228T=	NCBI36
NG_007406.1:g.24952A= , LRG_308:g.24952A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3075A=	ENSP00000460666.3:p.Gln1025=
ENST00000565038.2:c.*550A=	ENSP00000459882.2:n.*550A=
ENST00000566069.6:c.3069A=	ENSP00000459237.2:p.Gln1023=
ENST00000697377.2:c.2913A=	ENSP00000513286.2:p.Gln971=
ENST00000697379.2:c.3075A=	ENSP00000513287.2:p.Gln1025=
ENST00000561514.2:c.2184A=	ENSP00000460666.2:p.Gln728=
ENST00000697374.1:c.2184A=	ENSP00000513284.1:p.Gln728=
ENST00000697375.1:n.4416A=
ENST00000697376.1:c.2184A=	ENSP00000513285.1:p.Gln728=
ENST00000697377.1:c.2022A=	ENSP00000513286.1:p.Gln674=
ENST00000697378.1:n.3589A=
ENST00000697379.1:c.2184A=	ENSP00000513287.1:p.Gln728=
ENST00000697380.1:n.2361A=
ENST00000697381.1:n.1764A=
ENST00000697382.1:c.2184A=	ENSP00000513288.1:p.Gln728=
ENST00000697383.1:c.603A=	ENSP00000513289.1:p.Gln201=
ENST00000261584.9:c.3069A= MANE Select	ENSP00000261584.4:p.Gln1023=
ENST00000261584.8:c.3069A=	ENSP00000261584.4:p.Gln1023=
ENST00000568219.5:c.2184A=	ENSP00000454703.2:p.Gln728=
NM_024675.3:c.3069A= , LRG_308t1:c.3069A=	NP_078951.2:p.Gln1023=
XM_011545946.1:c.3075A=	XP_011544248.1:p.Gln1025=
XM_011545947.1:c.3075A=	XP_011544249.1:p.Gln1025=
XM_011545948.1:c.2184A=	XP_011544250.1:p.Gln728=
XR_950851.1:n.3865A=
XM_011545946.2:c.3075A=	XP_011544248.1:p.Gln1025=
XM_011545947.2:c.3075A=	XP_011544249.1:p.Gln1025=
XM_011545948.2:c.2184A=	XP_011544250.1:p.Gln728=
XM_017023671.1:c.3075A=	XP_016879160.1:p.Gln1025=
XM_017023672.2:c.3069A=	XP_016879161.1:p.Gln1023=
XM_017023673.2:c.3069A=	XP_016879162.1:p.Gln1023=
NM_024675.4:c.3069A= MANE Select	NP_078951.2:p.Gln1023=