Canonical Allele Identifier: CA7963335

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23603576A>G , CM000678.2:g.23603576A>G	GRCh38
NC_000016.9:g.23614897A>G , CM000678.1:g.23614897A>G	GRCh37
NC_000016.8:g.23522398A>G	NCBI36
NG_007406.1:g.42782T>C , LRG_308:g.42782T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3450T>C	ENSP00000460666.3:p.Thr1150=
ENST00000565038.2:c.*929T>C	ENSP00000459882.2:n.*929T>C
ENST00000566069.6:c.*79T>C	ENSP00000459237.2:n.*79T>C
ENST00000697377.2:c.3288T>C	ENSP00000513286.2:p.Thr1096=
ENST00000697379.2:c.3450T>C	ENSP00000513287.2:p.Thr1150=
ENST00000561514.2:c.2559T>C	ENSP00000460666.2:p.Thr853=
ENST00000697374.1:c.2559T>C	ENSP00000513284.1:p.Thr853=
ENST00000697375.1:n.4791T>C
ENST00000697376.1:c.*79T>C	ENSP00000513285.1:n.*79T>C
ENST00000697377.1:c.2397T>C	ENSP00000513286.1:p.Thr799=
ENST00000697378.1:n.3964T>C
ENST00000697379.1:c.2559T>C	ENSP00000513287.1:p.Thr853=
ENST00000697380.1:n.2648T>C
ENST00000697381.1:n.2139T>C
ENST00000697382.1:c.*221T>C	ENSP00000513288.1:n.*221T>C
ENST00000697383.1:c.978T>C	ENSP00000513289.1:p.Thr326=
ENST00000261584.9:c.3444T>C MANE Select	ENSP00000261584.4:p.Thr1148=
ENST00000261584.8:c.3444T>C	ENSP00000261584.4:p.Thr1148=
ENST00000566069.5:c.210T>C
ENST00000568219.5:c.2559T>C	ENSP00000454703.2:p.Thr853=
NM_024675.3:c.3444T>C , LRG_308t1:c.3444T>C	NP_078951.2:p.Thr1148=
XM_011545946.1:c.3450T>C	XP_011544248.1:p.Thr1150=
XM_011545947.1:c.*79T>C	XP_011544249.1:n.*79T>C
XM_011545948.1:c.2559T>C	XP_011544250.1:p.Thr853=
XR_950851.1:n.4152T>C
XM_011545946.2:c.3450T>C	XP_011544248.1:p.Thr1150=
XM_011545947.2:c.*79T>C	XP_011544249.1:n.*79T>C
XM_011545948.2:c.2559T>C	XP_011544250.1:p.Thr853=
XM_017023671.1:c.3213T>C	XP_016879160.1:p.Thr1071=
XM_017023672.2:c.3207T>C	XP_016879161.1:p.Thr1069=
XM_017023673.2:c.*79T>C	XP_016879162.1:n.*79T>C
NM_024675.4:c.3444T>C MANE Select	NP_078951.2:p.Thr1148=