Canonical Allele Identifier: CA7963801
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs515726108

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23636231C>T , CM000678.2:g.23636231C>T GRCh38
NC_000016.9:g.23647552C>T , CM000678.1:g.23647552C>T GRCh37
NC_000016.8:g.23555053C>T NCBI36
NG_007406.1:g.10127G>A , LRG_308:g.10127G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.321G>A ENSP00000460666.3:p.Glu107=
ENST00000565038.2:c.211+1619G>A ENSP00000459882.2:n.211+1619G>A
ENST00000566069.6:c.315G>A ENSP00000459237.2:p.Glu105=
ENST00000697377.2:c.321G>A ENSP00000513286.2:p.Glu107=
ENST00000697379.2:c.321G>A ENSP00000513287.2:p.Glu107=
ENST00000561514.2:c.-571G>A ENSP00000460666.2:n.-571G>A
ENST00000697374.1:c.-571G>A ENSP00000513284.1:n.-571G>A
ENST00000697375.1:n.1662G>A
ENST00000697376.1:c.-571G>A ENSP00000513285.1:n.-571G>A
ENST00000697377.1:c.-571G>A ENSP00000513286.1:n.-571G>A
ENST00000697378.1:n.835G>A
ENST00000697379.1:c.-571G>A ENSP00000513287.1:n.-571G>A
ENST00000697382.1:c.-571G>A ENSP00000513288.1:n.-571G>A
ENST00000697383.1:c.48+4879G>A ENSP00000513289.1:n.48+4879G>A
ENST00000697384.1:n.469G>A
ENST00000261584.9:c.315G>A MANE Select ENSP00000261584.4:p.Glu105=
ENST00000261584.8:c.315G>A ENSP00000261584.4:p.Glu105=
ENST00000565038.1:c.86+1619G>A
ENST00000567003.1:n.593G>A
ENST00000568219.5:c.-571G>A ENSP00000454703.2:n.-571G>A
NM_024675.3:c.315G>A , LRG_308t1:c.315G>A NP_078951.2:p.Glu105=
XM_011545946.1:c.321G>A XP_011544248.1:p.Glu107=
XM_011545947.1:c.321G>A XP_011544249.1:p.Glu107=
XM_011545948.1:c.-571G>A XP_011544250.1:n.-571G>A
XR_950851.1:n.1111G>A
XM_011545946.2:c.321G>A XP_011544248.1:p.Glu107=
XM_011545947.2:c.321G>A XP_011544249.1:p.Glu107=
XM_011545948.2:c.-571G>A XP_011544250.1:n.-571G>A
XM_017023671.1:c.321G>A XP_016879160.1:p.Glu107=
XM_017023672.2:c.315G>A XP_016879161.1:p.Glu105=
XM_017023673.2:c.315G>A XP_016879162.1:p.Glu105=
NM_024675.4:c.315G>A MANE Select NP_078951.2:p.Glu105=