Canonical Allele Identifier: CA395136237

Gene: PALB2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635809G>C , CM000678.2:g.23635809G>C	GRCh38
NC_000016.9:g.23647130G>C , CM000678.1:g.23647130G>C	GRCh37
NC_000016.8:g.23554631G>C	NCBI36
NG_007406.1:g.10549C>G , LRG_308:g.10549C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.743C>G	ENSP00000460666.3:p.Thr248Ser
ENST00000565038.2:c.211+2041C>G	ENSP00000459882.2:n.211+2041C>G
ENST00000566069.6:c.737C>G	ENSP00000459237.2:p.Thr246Ser
ENST00000697377.2:c.743C>G	ENSP00000513286.2:p.Thr248Ser
ENST00000697379.2:c.743C>G	ENSP00000513287.2:p.Thr248Ser
ENST00000561514.2:c.-149C>G	ENSP00000460666.2:n.-149C>G
ENST00000697374.1:c.-149C>G	ENSP00000513284.1:n.-149C>G
ENST00000697375.1:n.2084C>G
ENST00000697376.1:c.-149C>G	ENSP00000513285.1:n.-149C>G
ENST00000697377.1:c.-149C>G	ENSP00000513286.1:n.-149C>G
ENST00000697378.1:n.1257C>G
ENST00000697379.1:c.-149C>G	ENSP00000513287.1:n.-149C>G
ENST00000697382.1:c.-149C>G	ENSP00000513288.1:n.-149C>G
ENST00000697383.1:c.48+5301C>G	ENSP00000513289.1:n.48+5301C>G
ENST00000697384.1:n.891C>G
ENST00000261584.9:c.737C>G MANE Select	ENSP00000261584.4:p.Thr246Ser
ENST00000261584.8:c.737C>G	ENSP00000261584.4:p.Thr246Ser
ENST00000565038.1:c.86+2041C>G
ENST00000568219.5:c.-149C>G	ENSP00000454703.2:n.-149C>G
NM_024675.3:c.737C>G , LRG_308t1:c.737C>G	NP_078951.2:p.Thr246Ser
XM_011545946.1:c.743C>G	XP_011544248.1:p.Thr248Ser
XM_011545947.1:c.743C>G	XP_011544249.1:p.Thr248Ser
XM_011545948.1:c.-149C>G	XP_011544250.1:n.-149C>G
XR_950851.1:n.1533C>G
XM_011545946.2:c.743C>G	XP_011544248.1:p.Thr248Ser
XM_011545947.2:c.743C>G	XP_011544249.1:p.Thr248Ser
XM_011545948.2:c.-149C>G	XP_011544250.1:n.-149C>G
XM_017023671.1:c.743C>G	XP_016879160.1:p.Thr248Ser
XM_017023672.2:c.737C>G	XP_016879161.1:p.Thr246Ser
XM_017023673.2:c.737C>G	XP_016879162.1:p.Thr246Ser
NM_024675.4:c.737C>G MANE Select	NP_078951.2:p.Thr246Ser