Canonical Allele Identifier: CA2482057119
Gene: REN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159595C= , CM000663.2:g.204159595C= GRCh38
NC_000001.10:g.204128723C= , CM000663.1:g.204128723C= GRCh37
NC_000001.9:g.202395346C= NCBI36
NG_012122.1:g.11743G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.493G= MANE Select ENSP00000272190.8:p.Val165=
ENST00000638118.1:c.379G= ENSP00000490307.1:p.Val127=
ENST00000272190.8:c.493G= ENSP00000272190.8:p.Val165=
NM_000537.3:c.493G= NP_000528.1:p.Val165=
NM_000537.4:c.493G= MANE Select NP_000528.1:p.Val165=
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