Canonical Allele Identifier: CA344332270
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204124209T>A (hg19) chr1:g.204155081T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155081T>A , CM000663.2:g.204155081T>A GRCh38
NC_000001.10:g.204124209T>A , CM000663.1:g.204124209T>A GRCh37
NC_000001.9:g.202390832T>A NCBI36
NG_012122.1:g.16257A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.1156A>T MANE Select ENSP00000272190.8:p.Ile386Phe
ENST00000638118.1:c.1042A>T ENSP00000490307.1:p.Ile348Phe
ENST00000272190.8:c.1156A>T ENSP00000272190.8:p.Ile386Phe
NM_000537.3:c.1156A>T NP_000528.1:p.Ile386Phe
NM_000537.4:c.1156A>T MANE Select NP_000528.1:p.Ile386Phe
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