Canonical Allele Identifier: CA1258761123

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.68653266_68653267delinsCG , CM000664.2:g.68653266_68653267delinsCG GRCh38
NC_000002.11:g.68880398_68880399delinsCG , CM000664.1:g.68880398_68880399delinsCG GRCh37
NC_000002.10:g.68733902_68733903delinsCG NCBI36
NG_051312.1:g.14679_14680delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000303786.5:c.486-1614_486-1613delinsCG (PROKR1) MANE Select ENSP00000303775.4:n.486-1614_486-1613deli...
ENST00000303786.4:c.486-1614_486-1613delinsCG (PROKR1) ENSP00000303775.3:n.486-1614_486-1613deli...
ENST00000394342.2:c.486-1614_486-1613delinsCG (APLF) ENSP00000377874.2:n.486-1614_486-1613deli...
ENST00000627740.1:n.1198-1614_1198-1613delinsCG (APLF)
NM_138964.2:c.486-1614_486-1613delinsCG (PROKR1) NP_620414.1:n.486-1614_486-1613delinsCG
NM_138964.3:c.486-1614_486-1613delinsCG (PROKR1) NP_620414.1:n.486-1614_486-1613delinsCG
NM_138964.4:c.486-1614_486-1613delinsCG (PROKR1) MANE Select NP_620414.1:n.486-1614_486-1613delinsCG