Canonical Allele Identifier: CA2482055228
Gene: REN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155086G= , CM000663.2:g.204155086G= GRCh38
NC_000001.10:g.204124214G= , CM000663.1:g.204124214G= GRCh37
NC_000001.9:g.202390837G= NCBI36
NG_012122.1:g.16252C=

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.1151C= MANE Select ENSP00000272190.8:p.Thr384=
ENST00000638118.1:c.1037C= ENSP00000490307.1:p.Thr346=
ENST00000272190.8:c.1151C= ENSP00000272190.8:p.Thr384=
NM_000537.3:c.1151C= NP_000528.1:p.Thr384=
NM_000537.4:c.1151C= MANE Select NP_000528.1:p.Thr384=
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