Canonical Allele Identifier: CA344332286
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204124217G>T (hg19) chr1:g.204155089G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155089G>T , CM000663.2:g.204155089G>T GRCh38
NC_000001.10:g.204124217G>T , CM000663.1:g.204124217G>T GRCh37
NC_000001.9:g.202390840G>T NCBI36
NG_012122.1:g.16249C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.1148C>A MANE Select ENSP00000272190.8:p.Ala383Asp
ENST00000638118.1:c.1034C>A ENSP00000490307.1:p.Ala345Asp
ENST00000272190.8:c.1148C>A ENSP00000272190.8:p.Ala383Asp
NM_000537.3:c.1148C>A NP_000528.1:p.Ala383Asp
NM_000537.4:c.1148C>A MANE Select NP_000528.1:p.Ala383Asp
Search 100 bp 5'
Search 100 bp 3'