Canonical Allele Identifier: CA494180455

Gene: PALB2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23623052G>C , CM000678.2:g.23623052G>C	GRCh38
NC_000016.9:g.23634373G>C , CM000678.1:g.23634373G>C	GRCh37
NC_000016.8:g.23541874G>C	NCBI36
NG_007406.1:g.23306C>G , LRG_308:g.23306C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2919C>G	ENSP00000460666.3:p.Gly973=
ENST00000565038.2:c.*394C>G	ENSP00000459882.2:n.*394C>G
ENST00000566069.6:c.2913C>G	ENSP00000459237.2:p.Gly971=
ENST00000697377.2:c.2757C>G	ENSP00000513286.2:p.Gly919=
ENST00000697379.2:c.2919C>G	ENSP00000513287.2:p.Gly973=
ENST00000561514.2:c.2028C>G	ENSP00000460666.2:p.Gly676=
ENST00000697374.1:c.2028C>G	ENSP00000513284.1:p.Gly676=
ENST00000697375.1:n.4260C>G
ENST00000697376.1:c.2028C>G	ENSP00000513285.1:p.Gly676=
ENST00000697377.1:c.1866C>G	ENSP00000513286.1:p.Gly622=
ENST00000697378.1:n.3433C>G
ENST00000697379.1:c.2028C>G	ENSP00000513287.1:p.Gly676=
ENST00000697380.1:n.2205C>G
ENST00000697381.1:n.1608C>G
ENST00000697382.1:c.2028C>G	ENSP00000513288.1:p.Gly676=
ENST00000697383.1:c.447C>G	ENSP00000513289.1:p.Gly149=
ENST00000261584.9:c.2913C>G MANE Select	ENSP00000261584.4:p.Gly971=
ENST00000261584.8:c.2913C>G	ENSP00000261584.4:p.Gly971=
ENST00000568219.5:c.2028C>G	ENSP00000454703.2:p.Gly676=
NM_024675.3:c.2913C>G , LRG_308t1:c.2913C>G	NP_078951.2:p.Gly971=
XM_011545946.1:c.2919C>G	XP_011544248.1:p.Gly973=
XM_011545947.1:c.2919C>G	XP_011544249.1:p.Gly973=
XM_011545948.1:c.2028C>G	XP_011544250.1:p.Gly676=
XR_950851.1:n.3709C>G
XM_011545946.2:c.2919C>G	XP_011544248.1:p.Gly973=
XM_011545947.2:c.2919C>G	XP_011544249.1:p.Gly973=
XM_011545948.2:c.2028C>G	XP_011544250.1:p.Gly676=
XM_017023671.1:c.2919C>G	XP_016879160.1:p.Gly973=
XM_017023672.2:c.2913C>G	XP_016879161.1:p.Gly971=
XM_017023673.2:c.2913C>G	XP_016879162.1:p.Gly971=
NM_024675.4:c.2913C>G MANE Select	NP_078951.2:p.Gly971=