Canonical Allele Identifier: CA344332277
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204124212A>C (hg19) chr1:g.204155084A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155084A>C , CM000663.2:g.204155084A>C GRCh38
NC_000001.10:g.204124212A>C , CM000663.1:g.204124212A>C GRCh37
NC_000001.9:g.202390835A>C NCBI36
NG_012122.1:g.16254T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.1153T>G MANE Select ENSP00000272190.8:p.Phe385Val
ENST00000638118.1:c.1039T>G ENSP00000490307.1:p.Phe347Val
ENST00000272190.8:c.1153T>G ENSP00000272190.8:p.Phe385Val
NM_000537.3:c.1153T>G NP_000528.1:p.Phe385Val
NM_000537.4:c.1153T>G MANE Select NP_000528.1:p.Phe385Val
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