Canonical Allele Identifier: CA1258761094

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.68653214_68653215delinsCT , CM000664.2:g.68653214_68653215delinsCT GRCh38
NC_000002.11:g.68880346_68880347delinsCT , CM000664.1:g.68880346_68880347delinsCT GRCh37
NC_000002.10:g.68733850_68733851delinsCT NCBI36
NG_051312.1:g.14627_14628delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000303786.5:c.486-1666_486-1665delinsCT (PROKR1) MANE Select ENSP00000303775.4:n.486-1666_486-1665deli...
ENST00000303786.4:c.486-1666_486-1665delinsCT (PROKR1) ENSP00000303775.3:n.486-1666_486-1665deli...
ENST00000394342.2:c.486-1666_486-1665delinsCT (APLF) ENSP00000377874.2:n.486-1666_486-1665deli...
ENST00000627740.1:n.1198-1666_1198-1665delinsCT (APLF)
NM_138964.2:c.486-1666_486-1665delinsCT (PROKR1) NP_620414.1:n.486-1666_486-1665delinsCT
NM_138964.3:c.486-1666_486-1665delinsCT (PROKR1) NP_620414.1:n.486-1666_486-1665delinsCT
NM_138964.4:c.486-1666_486-1665delinsCT (PROKR1) MANE Select NP_620414.1:n.486-1666_486-1665delinsCT