Canonical Allele Identifier: CA2482059825
Gene: REN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204166246_204166249delinsGAGC , CM000663.2:g.204166246_204166249delinsGAGC GRCh38
NC_000001.10:g.204135374_204135377delinsGAGC , CM000663.1:g.204135374_204135377delinsGAGC GRCh37
NC_000001.9:g.202401997_202402000delinsGAGC NCBI36
NG_012122.1:g.5089_5092delinsGCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.45_48delinsGCTC MANE Select ENSP00000272190.8:p.Leu15=
ENST00000638118.1:c.-16-4086_-16-4083delinsGCTC ENSP00000490307.1:n.-16-4086_-16-4083delinsGCTC
ENST00000272190.8:c.45_48delinsGCTC ENSP00000272190.8:p.Leu15=
NM_000537.3:c.45_48delinsGCTC NP_000528.1:p.Leu15=
NM_000537.4:c.45_48delinsGCTC MANE Select NP_000528.1:p.Leu15=
Search 100 bp 5'
Search 100 bp 3'