Canonical Allele Identifier: CA892390676

Linked Data

dbSNP Id: rs1303289325
gnomAD v3: 2-68653266-C-A
gnomAD v4: 2-68653266-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.68653266C>A , CM000664.2:g.68653266C>A GRCh38
NC_000002.11:g.68880398C>A , CM000664.1:g.68880398C>A GRCh37
NC_000002.10:g.68733902C>A NCBI36
NG_051312.1:g.14679C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000303786.5:c.486-1614C>A (PROKR1) MANE Select ENSP00000303775.4:n.486-1614C>A
ENST00000303786.4:c.486-1614C>A (PROKR1) ENSP00000303775.3:n.486-1614C>A
ENST00000394342.2:c.486-1614C>A (APLF) ENSP00000377874.2:n.486-1614C>A
ENST00000627740.1:n.1198-1614C>A (APLF)
NM_138964.2:c.486-1614C>A (PROKR1) NP_620414.1:n.486-1614C>A
NM_138964.3:c.486-1614C>A (PROKR1) NP_620414.1:n.486-1614C>A
NM_138964.4:c.486-1614C>A (PROKR1) MANE Select NP_620414.1:n.486-1614C>A