Canonical Allele Identifier: CA494461300

Gene: PALB2

Linked Data

• MyVariant Identifiers: chr16:g.23646328T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635007T>G , CM000678.2:g.23635007T>G	GRCh38
NC_000016.9:g.23646328T>G , CM000678.1:g.23646328T>G	GRCh37
NC_000016.8:g.23553829T>G	NCBI36
NG_007406.1:g.11351A>C , LRG_308:g.11351A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1545A>C	ENSP00000460666.3:p.Thr515=
ENST00000565038.2:c.211+2843A>C	ENSP00000459882.2:n.211+2843A>C
ENST00000566069.6:c.1539A>C	ENSP00000459237.2:p.Thr513=
ENST00000697377.2:c.1545A>C	ENSP00000513286.2:p.Thr515=
ENST00000697379.2:c.1545A>C	ENSP00000513287.2:p.Thr515=
ENST00000561514.2:c.654A>C	ENSP00000460666.2:p.Thr218=
ENST00000697374.1:c.654A>C	ENSP00000513284.1:p.Thr218=
ENST00000697375.1:n.2886A>C
ENST00000697376.1:c.654A>C	ENSP00000513285.1:p.Thr218=
ENST00000697377.1:c.654A>C	ENSP00000513286.1:p.Thr218=
ENST00000697378.1:n.2059A>C
ENST00000697379.1:c.654A>C	ENSP00000513287.1:p.Thr218=
ENST00000697382.1:c.654A>C	ENSP00000513288.1:p.Thr218=
ENST00000697383.1:c.49-5732A>C	ENSP00000513289.1:n.49-5732A>C
ENST00000697384.1:n.1693A>C
ENST00000261584.9:c.1539A>C MANE Select	ENSP00000261584.4:p.Thr513=
ENST00000261584.8:c.1539A>C	ENSP00000261584.4:p.Thr513=
ENST00000565038.1:c.86+2843A>C
ENST00000568219.5:c.654A>C	ENSP00000454703.2:p.Thr218=
NM_024675.3:c.1539A>C , LRG_308t1:c.1539A>C	NP_078951.2:p.Thr513=
XM_011545946.1:c.1545A>C	XP_011544248.1:p.Thr515=
XM_011545947.1:c.1545A>C	XP_011544249.1:p.Thr515=
XM_011545948.1:c.654A>C	XP_011544250.1:p.Thr218=
XR_950851.1:n.2335A>C
XM_011545946.2:c.1545A>C	XP_011544248.1:p.Thr515=
XM_011545947.2:c.1545A>C	XP_011544249.1:p.Thr515=
XM_011545948.2:c.654A>C	XP_011544250.1:p.Thr218=
XM_017023671.1:c.1545A>C	XP_016879160.1:p.Thr515=
XM_017023672.2:c.1539A>C	XP_016879161.1:p.Thr513=
XM_017023673.2:c.1539A>C	XP_016879162.1:p.Thr513=
NM_024675.4:c.1539A>C MANE Select	NP_078951.2:p.Thr513=