Canonical Allele Identifier: CA2482057125
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159604G= , CM000663.2:g.204159604G= GRCh38
NC_000001.10:g.204128732G= , CM000663.1:g.204128732G= GRCh37
NC_000001.9:g.202395355G= NCBI36
NG_012122.1:g.11734C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.493-9C= MANE Select ENSP00000272190.8:n.493-9C=
ENST00000638118.1:c.379-9C= ENSP00000490307.1:n.379-9C=
ENST00000272190.8:c.493-9C= ENSP00000272190.8:n.493-9C=
NM_000537.3:c.493-9C= NP_000528.1:n.493-9C=
NM_000537.4:c.493-9C= MANE Select NP_000528.1:n.493-9C=