Canonical Allele Identifier: CA344332288
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204124218C>G (hg19) chr1:g.204155090C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155090C>G , CM000663.2:g.204155090C>G GRCh38
NC_000001.10:g.204124218C>G , CM000663.1:g.204124218C>G GRCh37
NC_000001.9:g.202390841C>G NCBI36
NG_012122.1:g.16248G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.1147G>C MANE Select ENSP00000272190.8:p.Ala383Pro
ENST00000638118.1:c.1033G>C ENSP00000490307.1:p.Ala345Pro
ENST00000272190.8:c.1147G>C ENSP00000272190.8:p.Ala383Pro
NM_000537.3:c.1147G>C NP_000528.1:p.Ala383Pro
NM_000537.4:c.1147G>C MANE Select NP_000528.1:p.Ala383Pro
Search 100 bp 5'
Search 100 bp 3'