Canonical Allele Identifier: CA1143885352
Gene: REN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155136G= , CM000663.2:g.204155136G= GRCh38
NC_000001.10:g.204124264G= , CM000663.1:g.204124264G= GRCh37
NC_000001.9:g.202390887G= NCBI36
NG_012122.1:g.16202C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.1101C= MANE Select ENSP00000272190.8:p.His367=
ENST00000638118.1:c.987C= ENSP00000490307.1:p.His329=
ENST00000272190.8:c.1101C= ENSP00000272190.8:p.His367=
NM_000537.3:c.1101C= NP_000528.1:p.His367=
NM_000537.4:c.1101C= MANE Select NP_000528.1:p.His367=
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