Canonical Allele Identifier: CA344337978

Gene: REN

Linked Data

• MyVariant Identifiers: chr1:g.204128596G>C (hg19) ; chr1:g.204159468G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204159468G>C , CM000663.2:g.204159468G>C	GRCh38
NC_000001.10:g.204128596G>C , CM000663.1:g.204128596G>C	GRCh37
NC_000001.9:g.202395219G>C	NCBI36
NG_012122.1:g.11870C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272190.9:c.620C>G MANE Select	ENSP00000272190.8:p.Thr207Ser
ENST00000638118.1:c.506C>G	ENSP00000490307.1:p.Thr169Ser
ENST00000272190.8:c.620C>G	ENSP00000272190.8:p.Thr207Ser
NM_000537.3:c.620C>G	NP_000528.1:p.Thr207Ser
NM_000537.4:c.620C>G MANE Select	NP_000528.1:p.Thr207Ser