Canonical Allele Identifier: CA2482059407
Gene: REN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204165234G= , CM000663.2:g.204165234G= GRCh38
NC_000001.10:g.204134362G= , CM000663.1:g.204134362G= GRCh37
NC_000001.9:g.202400985G= NCBI36
NG_012122.1:g.6104C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.98+962C= MANE Select ENSP00000272190.8:n.98+962C=
ENST00000638118.1:c.-16-3071C= ENSP00000490307.1:n.-16-3071C=
ENST00000272190.8:c.98+962C= ENSP00000272190.8:n.98+962C=
NM_000537.3:c.98+962C= NP_000528.1:n.98+962C=
NM_000537.4:c.98+962C= MANE Select NP_000528.1:n.98+962C=
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