Canonical Allele Identifier: CA923726356
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621401_23621402delinsCG , CM000678.2:g.23621401_23621402delinsCG GRCh38
NC_000016.9:g.23632722_23632723delinsCG , CM000678.1:g.23632722_23632723delinsCG GRCh37
NC_000016.8:g.23540223_23540224delinsCG NCBI36
NG_007406.1:g.24956_24957delinsCG , LRG_308:g.24956_24957delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3079_3080delinsCG ENSP00000460666.3:p.Ala1027Arg
ENST00000565038.2:c.*554_*555delinsCG ENSP00000459882.2:n.*554_*555delinsCG
ENST00000566069.6:c.3073_3074delinsCG ENSP00000459237.2:p.Ala1025Arg
ENST00000697377.2:c.2917_2918delinsCG ENSP00000513286.2:p.Ala973Arg
ENST00000697379.2:c.3079_3080delinsCG ENSP00000513287.2:p.Ala1027Arg
ENST00000561514.2:c.2188_2189delinsCG ENSP00000460666.2:p.Ala730Arg
ENST00000697374.1:c.2188_2189delinsCG ENSP00000513284.1:p.Ala730Arg
ENST00000697375.1:n.4420_4421delinsCG
ENST00000697376.1:c.2188_2189delinsCG ENSP00000513285.1:p.Ala730Arg
ENST00000697377.1:c.2026_2027delinsCG ENSP00000513286.1:p.Ala676Arg
ENST00000697378.1:n.3593_3594delinsCG
ENST00000697379.1:c.2188_2189delinsCG ENSP00000513287.1:p.Ala730Arg
ENST00000697380.1:n.2365_2366delinsCG
ENST00000697381.1:n.1768_1769delinsCG
ENST00000697382.1:c.2188_2189delinsCG ENSP00000513288.1:p.Ala730Arg
ENST00000697383.1:c.607_608delinsCG ENSP00000513289.1:p.Ala203Arg
ENST00000261584.9:c.3073_3074delinsCG MANE Select ENSP00000261584.4:p.Ala1025Arg
ENST00000261584.8:c.3073_3074delinsCG ENSP00000261584.4:p.Ala1025Arg
ENST00000568219.5:c.2188_2189delinsCG ENSP00000454703.2:p.Ala730Arg
NM_024675.3:c.3073_3074delinsCG , LRG_308t1:c.3073_3074delinsCG NP_078951.2:p.Ala1025Arg
XM_011545946.1:c.3079_3080delinsCG XP_011544248.1:p.Ala1027Arg
XM_011545947.1:c.3079_3080delinsCG XP_011544249.1:p.Ala1027Arg
XM_011545948.1:c.2188_2189delinsCG XP_011544250.1:p.Ala730Arg
XR_950851.1:n.3869_3870delinsCG
XM_011545946.2:c.3079_3080delinsCG XP_011544248.1:p.Ala1027Arg
XM_011545947.2:c.3079_3080delinsCG XP_011544249.1:p.Ala1027Arg
XM_011545948.2:c.2188_2189delinsCG XP_011544250.1:p.Ala730Arg
XM_017023671.1:c.3079_3080delinsCG XP_016879160.1:p.Ala1027Arg
XM_017023672.2:c.3073_3074delinsCG XP_016879161.1:p.Ala1025Arg
XM_017023673.2:c.3073_3074delinsCG XP_016879162.1:p.Ala1025Arg
NM_024675.4:c.3073_3074delinsCG MANE Select NP_078951.2:p.Ala1025Arg