Canonical Allele Identifier: CA2213423874
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23630181_23630182delinsTC , CM000678.2:g.23630181_23630182delinsTC GRCh38
NC_000016.9:g.23641502_23641503delinsTC , CM000678.1:g.23641502_23641503delinsTC GRCh37
NC_000016.8:g.23549003_23549004delinsTC NCBI36
NG_007406.1:g.16176_16177delinsGA , LRG_308:g.16176_16177delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.1978_1979delinsGA ENSP00000460666.3:p.Glu660=
ENST00000565038.2:c.212-907_212-906delinsGA ENSP00000459882.2:n.212-907_212-906delinsGA
ENST00000566069.6:c.1972_1973delinsGA ENSP00000459237.2:p.Glu658=
ENST00000697377.2:c.1978_1979delinsGA ENSP00000513286.2:p.Glu660=
ENST00000697379.2:c.1978_1979delinsGA ENSP00000513287.2:p.Glu660=
ENST00000561514.2:c.1087_1088delinsGA ENSP00000460666.2:p.Glu363=
ENST00000697374.1:c.1087_1088delinsGA ENSP00000513284.1:p.Glu363=
ENST00000697375.1:n.3319_3320delinsGA
ENST00000697376.1:c.1087_1088delinsGA ENSP00000513285.1:p.Glu363=
ENST00000697377.1:c.1087_1088delinsGA ENSP00000513286.1:p.Glu363=
ENST00000697378.1:n.2492_2493delinsGA
ENST00000697379.1:c.1087_1088delinsGA ENSP00000513287.1:p.Glu363=
ENST00000697380.1:n.900_901delinsGA
ENST00000697381.1:n.667_668delinsGA
ENST00000697382.1:c.1087_1088delinsGA ENSP00000513288.1:p.Glu363=
ENST00000697383.1:c.49-907_49-906delinsGA ENSP00000513289.1:n.49-907_49-906delinsGA
ENST00000697384.1:n.2126_2127delinsGA
ENST00000261584.9:c.1972_1973delinsGA MANE Select ENSP00000261584.4:p.Glu658=
ENST00000261584.8:c.1972_1973delinsGA ENSP00000261584.4:p.Glu658=
ENST00000565038.1:c.87-907_87-906delinsGA
ENST00000568219.5:c.1087_1088delinsGA ENSP00000454703.2:p.Glu363=
NM_024675.3:c.1972_1973delinsGA , LRG_308t1:c.1972_1973delinsGA NP_078951.2:p.Glu658=
XM_011545946.1:c.1978_1979delinsGA XP_011544248.1:p.Glu660=
XM_011545947.1:c.1978_1979delinsGA XP_011544249.1:p.Glu660=
XM_011545948.1:c.1087_1088delinsGA XP_011544250.1:p.Glu363=
XR_950851.1:n.2768_2769delinsGA
XM_011545946.2:c.1978_1979delinsGA XP_011544248.1:p.Glu660=
XM_011545947.2:c.1978_1979delinsGA XP_011544249.1:p.Glu660=
XM_011545948.2:c.1087_1088delinsGA XP_011544250.1:p.Glu363=
XM_017023671.1:c.1978_1979delinsGA XP_016879160.1:p.Glu660=
XM_017023672.2:c.1972_1973delinsGA XP_016879161.1:p.Glu658=
XM_017023673.2:c.1972_1973delinsGA XP_016879162.1:p.Glu658=
NM_024675.4:c.1972_1973delinsGA MANE Select NP_078951.2:p.Glu658=