Canonical Allele Identifier: CA494180186
Gene: PALB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621449_23621450insC , CM000678.2:g.23621449_23621450insC GRCh38
NC_000016.9:g.23632770_23632771insC , CM000678.1:g.23632770_23632771insC GRCh37
NC_000016.8:g.23540271_23540272insC NCBI36
NG_007406.1:g.24908_24909insG , LRG_308:g.24908_24909insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3031_3032insG ENSP00000460666.3:p.Pro1011ArgfsTer2
ENST00000565038.2:c.*506_*507insG ENSP00000459882.2:n.*506_*507insG
ENST00000566069.6:c.3025_3026insG ENSP00000459237.2:p.Pro1009ArgfsTer2
ENST00000697377.2:c.2869_2870insG ENSP00000513286.2:p.Pro957ArgfsTer2
ENST00000697379.2:c.3031_3032insG ENSP00000513287.2:p.Pro1011ArgfsTer2
ENST00000561514.2:c.2140_2141insG ENSP00000460666.2:p.Pro714ArgfsTer2
ENST00000697374.1:c.2140_2141insG ENSP00000513284.1:p.Pro714ArgfsTer2
ENST00000697375.1:n.4372_4373insG
ENST00000697376.1:c.2140_2141insG ENSP00000513285.1:p.Pro714ArgfsTer2
ENST00000697377.1:c.1978_1979insG ENSP00000513286.1:p.Pro660ArgfsTer2
ENST00000697378.1:n.3545_3546insG
ENST00000697379.1:c.2140_2141insG ENSP00000513287.1:p.Pro714ArgfsTer2
ENST00000697380.1:n.2317_2318insG
ENST00000697381.1:n.1720_1721insG
ENST00000697382.1:c.2140_2141insG ENSP00000513288.1:p.Pro714ArgfsTer2
ENST00000697383.1:c.559_560insG ENSP00000513289.1:p.Pro187ArgfsTer2
ENST00000261584.9:c.3025_3026insG MANE Select ENSP00000261584.4:p.Pro1009ArgfsTer2
ENST00000261584.8:c.3025_3026insG ENSP00000261584.4:p.Pro1009ArgfsTer2
ENST00000568219.5:c.2140_2141insG ENSP00000454703.2:p.Pro714ArgfsTer2
NM_024675.3:c.3025_3026insG , LRG_308t1:c.3025_3026insG NP_078951.2:p.Pro1009ArgfsTer2
XM_011545946.1:c.3031_3032insG XP_011544248.1:p.Pro1011ArgfsTer2
XM_011545947.1:c.3031_3032insG XP_011544249.1:p.Pro1011ArgfsTer2
XM_011545948.1:c.2140_2141insG XP_011544250.1:p.Pro714ArgfsTer2
XR_950851.1:n.3821_3822insG
XM_011545946.2:c.3031_3032insG XP_011544248.1:p.Pro1011ArgfsTer2
XM_011545947.2:c.3031_3032insG XP_011544249.1:p.Pro1011ArgfsTer2
XM_011545948.2:c.2140_2141insG XP_011544250.1:p.Pro714ArgfsTer2
XM_017023671.1:c.3031_3032insG XP_016879160.1:p.Pro1011ArgfsTer2
XM_017023672.2:c.3025_3026insG XP_016879161.1:p.Pro1009ArgfsTer2
XM_017023673.2:c.3025_3026insG XP_016879162.1:p.Pro1009ArgfsTer2
NM_024675.4:c.3025_3026insG MANE Select NP_078951.2:p.Pro1009ArgfsTer2