Canonical Allele Identifier: CA1258761116

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.68653256G= , CM000664.2:g.68653256G= GRCh38
NC_000002.11:g.68880388G= , CM000664.1:g.68880388G= GRCh37
NC_000002.10:g.68733892G= NCBI36
NG_051312.1:g.14669G=

Transcript Alleles

HGVS Amino-acid change
ENST00000303786.5:c.486-1624G= (PROKR1) MANE Select ENSP00000303775.4:n.486-1624G=
ENST00000303786.4:c.486-1624G= (PROKR1) ENSP00000303775.3:n.486-1624G=
ENST00000394342.2:c.486-1624G= (APLF) ENSP00000377874.2:n.486-1624G=
ENST00000627740.1:n.1198-1624G= (APLF)
NM_138964.2:c.486-1624G= (PROKR1) NP_620414.1:n.486-1624G=
NM_138964.3:c.486-1624G= (PROKR1) NP_620414.1:n.486-1624G=
NM_138964.4:c.486-1624G= (PROKR1) MANE Select NP_620414.1:n.486-1624G=