Canonical Allele Identifier: CA2741477851

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.29821540_29821541insA , CM000678.2:g.29821540_29821541insA GRCh38
NC_000016.9:g.29832861_29832862insA , CM000678.1:g.29832861_29832862insA GRCh37
NC_000016.8:g.29740362_29740363insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000320330.8:c.*1786_*1787insA (PAGR1) MANE Select ENSP00000326519.6:n.*1786_*1787insA
ENST00000357402.10:c.-36+1030_-36+1031insA (MVP) MANE Select ENSP00000349977.5:n.-36+1030_-36+1031insA
ENST00000357402.9:c.-36+1030_-36+1031insA (MVP) ENSP00000349977.5:n.-36+1030_-36+1031insA
ENST00000395353.5:c.-77+1030_-77+1031insA (MVP) ENSP00000378760.1:n.-77+1030_-77+1031insA
ENST00000562285.1:c.402+1638_402+1639insA
ENST00000562463.5:c.-36+1030_-36+1031insA (MVP) ENSP00000457734.1:n.-36+1030_-36+1031insA
ENST00000563096.1:n.45+1030_45+1031insA (MVP)
ENST00000563558.5:c.-77+1030_-77+1031insA (MVP) ENSP00000454825.1:n.-77+1030_-77+1031insA
ENST00000563915.5:c.-77+1030_-77+1031insA (MVP) ENSP00000455819.1:n.-77+1030_-77+1031insA
ENST00000565164.1:c.-36+167_-36+168insA (MVP) ENSP00000454819.1:n.-36+167_-36+168insA
ENST00000565830.5:n.34+1030_34+1031insA (MVP)
ENST00000566066.5:c.-228+1030_-228+1031insA (MVP) ENSP00000455186.1:n.-228+1030_-228+1031insA
ENST00000566859.5:c.-36+1030_-36+1031insA (MVP) ENSP00000455741.1:n.-36+1030_-36+1031insA
ENST00000569887.1:c.-36+1030_-36+1031insA (MVP) ENSP00000455532.1:n.-36+1030_-36+1031insA
ENST00000570234.5:c.-146+149_-146+150insA (MVP) ENSP00000456291.1:n.-146+149_-146+150insA
NM_005115.4:c.-36+1030_-36+1031insA (MVP) NP_005106.2:n.-36+1030_-36+1031insA
NM_017458.3:c.-77+1030_-77+1031insA (MVP) NP_059447.2:n.-77+1030_-77+1031insA
NM_024516.3:c.*1786_*1787insA (PAGR1) NP_078792.1:n.*1786_*1787insA
NM_005115.5:c.-36+1030_-36+1031insA (MVP) MANE Select NP_005106.2:n.-36+1030_-36+1031insA
NM_024516.4:c.*1786_*1787insA (PAGR1) MANE Select NP_078792.1:n.*1786_*1787insA