Canonical Allele Identifier: CA2213409868
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621400_23621401delinsAG , CM000678.2:g.23621400_23621401delinsAG GRCh38
NC_000016.9:g.23632721_23632722delinsAG , CM000678.1:g.23632721_23632722delinsAG GRCh37
NC_000016.8:g.23540222_23540223delinsAG NCBI36
NG_007406.1:g.24957_24958delinsCT , LRG_308:g.24957_24958delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3080_3081delinsCT ENSP00000460666.3:p.Ala1027=
ENST00000565038.2:c.*555_*556delinsCT ENSP00000459882.2:n.*555_*556delinsCT
ENST00000566069.6:c.3074_3075delinsCT ENSP00000459237.2:p.Ala1025=
ENST00000697377.2:c.2918_2919delinsCT ENSP00000513286.2:p.Ala973=
ENST00000697379.2:c.3080_3081delinsCT ENSP00000513287.2:p.Ala1027=
ENST00000561514.2:c.2189_2190delinsCT ENSP00000460666.2:p.Ala730=
ENST00000697374.1:c.2189_2190delinsCT ENSP00000513284.1:p.Ala730=
ENST00000697375.1:n.4421_4422delinsCT
ENST00000697376.1:c.2189_2190delinsCT ENSP00000513285.1:p.Ala730=
ENST00000697377.1:c.2027_2028delinsCT ENSP00000513286.1:p.Ala676=
ENST00000697378.1:n.3594_3595delinsCT
ENST00000697379.1:c.2189_2190delinsCT ENSP00000513287.1:p.Ala730=
ENST00000697380.1:n.2366_2367delinsCT
ENST00000697381.1:n.1769_1770delinsCT
ENST00000697382.1:c.2189_2190delinsCT ENSP00000513288.1:p.Ala730=
ENST00000697383.1:c.608_609delinsCT ENSP00000513289.1:p.Ala203=
ENST00000261584.9:c.3074_3075delinsCT MANE Select ENSP00000261584.4:p.Ala1025=
ENST00000261584.8:c.3074_3075delinsCT ENSP00000261584.4:p.Ala1025=
ENST00000568219.5:c.2189_2190delinsCT ENSP00000454703.2:p.Ala730=
NM_024675.3:c.3074_3075delinsCT , LRG_308t1:c.3074_3075delinsCT NP_078951.2:p.Ala1025=
XM_011545946.1:c.3080_3081delinsCT XP_011544248.1:p.Ala1027=
XM_011545947.1:c.3080_3081delinsCT XP_011544249.1:p.Ala1027=
XM_011545948.1:c.2189_2190delinsCT XP_011544250.1:p.Ala730=
XR_950851.1:n.3870_3871delinsCT
XM_011545946.2:c.3080_3081delinsCT XP_011544248.1:p.Ala1027=
XM_011545947.2:c.3080_3081delinsCT XP_011544249.1:p.Ala1027=
XM_011545948.2:c.2189_2190delinsCT XP_011544250.1:p.Ala730=
XM_017023671.1:c.3080_3081delinsCT XP_016879160.1:p.Ala1027=
XM_017023672.2:c.3074_3075delinsCT XP_016879161.1:p.Ala1025=
XM_017023673.2:c.3074_3075delinsCT XP_016879162.1:p.Ala1025=
NM_024675.4:c.3074_3075delinsCT MANE Select NP_078951.2:p.Ala1025=