Canonical Allele Identifier: CA1258761102

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.68653230A= , CM000664.2:g.68653230A= GRCh38
NC_000002.11:g.68880362A= , CM000664.1:g.68880362A= GRCh37
NC_000002.10:g.68733866A= NCBI36
NG_051312.1:g.14643A=

Transcript Alleles

HGVS Amino-acid change
ENST00000303786.5:c.486-1650A= (PROKR1) MANE Select ENSP00000303775.4:n.486-1650A=
ENST00000303786.4:c.486-1650A= (PROKR1) ENSP00000303775.3:n.486-1650A=
ENST00000394342.2:c.486-1650A= (APLF) ENSP00000377874.2:n.486-1650A=
ENST00000627740.1:n.1198-1650A= (APLF)
NM_138964.2:c.486-1650A= (PROKR1) NP_620414.1:n.486-1650A=
NM_138964.3:c.486-1650A= (PROKR1) NP_620414.1:n.486-1650A=
NM_138964.4:c.486-1650A= (PROKR1) MANE Select NP_620414.1:n.486-1650A=