Canonical Allele Identifier: CA395125615
Gene: PALB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23629966T>A , CM000678.2:g.23629966T>A GRCh38
NC_000016.9:g.23641287T>A , CM000678.1:g.23641287T>A GRCh37
NC_000016.8:g.23548788T>A NCBI36
NG_007406.1:g.16392A>T , LRG_308:g.16392A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.2194A>T ENSP00000460666.3:p.Ile732Phe
ENST00000565038.2:c.212-691A>T ENSP00000459882.2:n.212-691A>T
ENST00000566069.6:c.2188A>T ENSP00000459237.2:p.Ile730Phe
ENST00000697377.2:c.2194A>T ENSP00000513286.2:p.Ile732Phe
ENST00000697379.2:c.2194A>T ENSP00000513287.2:p.Ile732Phe
ENST00000561514.2:c.1303A>T ENSP00000460666.2:p.Ile435Phe
ENST00000697374.1:c.1303A>T ENSP00000513284.1:p.Ile435Phe
ENST00000697375.1:n.3535A>T
ENST00000697376.1:c.1303A>T ENSP00000513285.1:p.Ile435Phe
ENST00000697377.1:c.1303A>T ENSP00000513286.1:p.Ile435Phe
ENST00000697378.1:n.2708A>T
ENST00000697379.1:c.1303A>T ENSP00000513287.1:p.Ile435Phe
ENST00000697380.1:n.1116A>T
ENST00000697381.1:n.883A>T
ENST00000697382.1:c.1303A>T ENSP00000513288.1:p.Ile435Phe
ENST00000697383.1:c.49-691A>T ENSP00000513289.1:n.49-691A>T
ENST00000697384.1:n.2342A>T
ENST00000261584.9:c.2188A>T MANE Select ENSP00000261584.4:p.Ile730Phe
ENST00000261584.8:c.2188A>T ENSP00000261584.4:p.Ile730Phe
ENST00000565038.1:c.87-691A>T
ENST00000568219.5:c.1303A>T ENSP00000454703.2:p.Ile435Phe
NM_024675.3:c.2188A>T , LRG_308t1:c.2188A>T NP_078951.2:p.Ile730Phe
XM_011545946.1:c.2194A>T XP_011544248.1:p.Ile732Phe
XM_011545947.1:c.2194A>T XP_011544249.1:p.Ile732Phe
XM_011545948.1:c.1303A>T XP_011544250.1:p.Ile435Phe
XR_950851.1:n.2984A>T
XM_011545946.2:c.2194A>T XP_011544248.1:p.Ile732Phe
XM_011545947.2:c.2194A>T XP_011544249.1:p.Ile732Phe
XM_011545948.2:c.1303A>T XP_011544250.1:p.Ile435Phe
XM_017023671.1:c.2194A>T XP_016879160.1:p.Ile732Phe
XM_017023672.2:c.2188A>T XP_016879161.1:p.Ile730Phe
XM_017023673.2:c.2188A>T XP_016879162.1:p.Ile730Phe
NM_024675.4:c.2188A>T MANE Select NP_078951.2:p.Ile730Phe