Canonical Allele Identifier: CA730338829
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1219099157
gnomAD v4: 1-204159279-AT-A
MyVariant Identifiers: chr1:g.204128408del (hg19) chr1:g.204159280del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159281del , CM000663.2:g.204159281del GRCh38
NC_000001.10:g.204128409del , CM000663.1:g.204128409del GRCh37
NC_000001.9:g.202395032del NCBI36
NG_012122.1:g.12058del

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.689+119del MANE Select ENSP00000272190.8:n.689+119del
ENST00000638118.1:c.575+119del ENSP00000490307.1:n.575+119del
ENST00000272190.8:c.689+119del ENSP00000272190.8:n.689+119del
NM_000537.3:c.689+119del NP_000528.1:n.689+119del
NM_000537.4:c.689+119del MANE Select NP_000528.1:n.689+119del
Search 100 bp 5'
Search 100 bp 3'