Canonical Allele Identifier: CA422833179

Gene: REN

Linked Data

• MyVariant Identifiers: chr1:g.204124225G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204155097G>C , CM000663.2:g.204155097G>C	GRCh38
NC_000001.10:g.204124225G>C , CM000663.1:g.204124225G>C	GRCh37
NC_000001.9:g.202390848G>C	NCBI36
NG_012122.1:g.16241C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272190.9:c.1140C>G MANE Select	ENSP00000272190.8:p.Ala380=
ENST00000638118.1:c.1026C>G	ENSP00000490307.1:p.Ala342=
ENST00000272190.8:c.1140C>G	ENSP00000272190.8:p.Ala380=
NM_000537.3:c.1140C>G	NP_000528.1:p.Ala380=
NM_000537.4:c.1140C>G MANE Select	NP_000528.1:p.Ala380=