Canonical Allele Identifier: CA2482057059
Gene: REN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159405T= , CM000663.2:g.204159405T= GRCh38
NC_000001.10:g.204128533T= , CM000663.1:g.204128533T= GRCh37
NC_000001.9:g.202395156T= NCBI36
NG_012122.1:g.11933A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.683A= MANE Select ENSP00000272190.8:p.Tyr228=
ENST00000638118.1:c.569A= ENSP00000490307.1:p.Tyr190=
ENST00000272190.8:c.683A= ENSP00000272190.8:p.Tyr228=
NM_000537.3:c.683A= NP_000528.1:p.Tyr228=
NM_000537.4:c.683A= MANE Select NP_000528.1:p.Tyr228=
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