Canonical Allele Identifier: CA35739608

Gene: REN

Linked Data

• dbSNP Id: rs1017446605
• MyVariant Identifiers: chr1:g.204134425A>C (hg19) ; chr1:g.204165297A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204165297A>C , CM000663.2:g.204165297A>C	GRCh38
NC_000001.10:g.204134425A>C , CM000663.1:g.204134425A>C	GRCh37
NC_000001.9:g.202401048A>C	NCBI36
NG_012122.1:g.6041T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272190.9:c.98+899T>G MANE Select	ENSP00000272190.8:n.98+899T>G
ENST00000638118.1:c.-16-3134T>G	ENSP00000490307.1:n.-16-3134T>G
ENST00000272190.8:c.98+899T>G	ENSP00000272190.8:n.98+899T>G
NM_000537.3:c.98+899T>G	NP_000528.1:n.98+899T>G
NM_000537.4:c.98+899T>G MANE Select	NP_000528.1:n.98+899T>G