Canonical Allele Identifier: CA2482055287
Gene: REN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155166A= , CM000663.2:g.204155166A= GRCh38
NC_000001.10:g.204124294A= , CM000663.1:g.204124294A= GRCh37
NC_000001.9:g.202390917A= NCBI36
NG_012122.1:g.16172T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.1071T= MANE Select ENSP00000272190.8:p.Ser357=
ENST00000638118.1:c.957T= ENSP00000490307.1:p.Ser319=
ENST00000272190.8:c.1071T= ENSP00000272190.8:p.Ser357=
NM_000537.3:c.1071T= NP_000528.1:p.Ser357=
NM_000537.4:c.1071T= MANE Select NP_000528.1:p.Ser357=
Search 100 bp 5'
Search 100 bp 3'