Canonical Allele Identifier: CA2213410384

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23621476C= , CM000678.2:g.23621476C=	GRCh38
NC_000016.9:g.23632797C= , CM000678.1:g.23632797C=	GRCh37
NC_000016.8:g.23540298C=	NCBI36
NG_007406.1:g.24882G= , LRG_308:g.24882G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3005G=	ENSP00000460666.3:p.Gly1002=
ENST00000565038.2:c.*480G=	ENSP00000459882.2:n.*480G=
ENST00000566069.6:c.2999G=	ENSP00000459237.2:p.Gly1000=
ENST00000697377.2:c.2843G=	ENSP00000513286.2:p.Gly948=
ENST00000697379.2:c.3005G=	ENSP00000513287.2:p.Gly1002=
ENST00000561514.2:c.2114G=	ENSP00000460666.2:p.Gly705=
ENST00000697374.1:c.2114G=	ENSP00000513284.1:p.Gly705=
ENST00000697375.1:n.4346G=
ENST00000697376.1:c.2114G=	ENSP00000513285.1:p.Gly705=
ENST00000697377.1:c.1952G=	ENSP00000513286.1:p.Gly651=
ENST00000697378.1:n.3519G=
ENST00000697379.1:c.2114G=	ENSP00000513287.1:p.Gly705=
ENST00000697380.1:n.2291G=
ENST00000697381.1:n.1694G=
ENST00000697382.1:c.2114G=	ENSP00000513288.1:p.Gly705=
ENST00000697383.1:c.533G=	ENSP00000513289.1:p.Gly178=
ENST00000261584.9:c.2999G= MANE Select	ENSP00000261584.4:p.Gly1000=
ENST00000261584.8:c.2999G=	ENSP00000261584.4:p.Gly1000=
ENST00000568219.5:c.2114G=	ENSP00000454703.2:p.Gly705=
NM_024675.3:c.2999G= , LRG_308t1:c.2999G=	NP_078951.2:p.Gly1000=
XM_011545946.1:c.3005G=	XP_011544248.1:p.Gly1002=
XM_011545947.1:c.3005G=	XP_011544249.1:p.Gly1002=
XM_011545948.1:c.2114G=	XP_011544250.1:p.Gly705=
XR_950851.1:n.3795G=
XM_011545946.2:c.3005G=	XP_011544248.1:p.Gly1002=
XM_011545947.2:c.3005G=	XP_011544249.1:p.Gly1002=
XM_011545948.2:c.2114G=	XP_011544250.1:p.Gly705=
XM_017023671.1:c.3005G=	XP_016879160.1:p.Gly1002=
XM_017023672.2:c.2999G=	XP_016879161.1:p.Gly1000=
XM_017023673.2:c.2999G=	XP_016879162.1:p.Gly1000=
NM_024675.4:c.2999G= MANE Select	NP_078951.2:p.Gly1000=