Canonical Allele Identifier: CA1149074997
Gene: REN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159403T= , CM000663.2:g.204159403T= GRCh38
NC_000001.10:g.204128531T= , CM000663.1:g.204128531T= GRCh37
NC_000001.9:g.202395154T= NCBI36
NG_012122.1:g.11935A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.685A= MANE Select ENSP00000272190.8:p.Asn229=
ENST00000638118.1:c.571A= ENSP00000490307.1:p.Asn191=
ENST00000272190.8:c.685A= ENSP00000272190.8:p.Asn229=
NM_000537.3:c.685A= NP_000528.1:p.Asn229=
NM_000537.4:c.685A= MANE Select NP_000528.1:p.Asn229=
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