Canonical Allele Identifier: CA344337709

Gene: REN

Linked Data

• MyVariant Identifiers: chr1:g.204128549C>A (hg19) ; chr1:g.204159421C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204159421C>A , CM000663.2:g.204159421C>A	GRCh38
NC_000001.10:g.204128549C>A , CM000663.1:g.204128549C>A	GRCh37
NC_000001.9:g.202395172C>A	NCBI36
NG_012122.1:g.11917G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272190.9:c.667G>T MANE Select	ENSP00000272190.8:p.Val223Phe
ENST00000638118.1:c.553G>T	ENSP00000490307.1:p.Val185Phe
ENST00000272190.8:c.667G>T	ENSP00000272190.8:p.Val223Phe
NM_000537.3:c.667G>T	NP_000528.1:p.Val223Phe
NM_000537.4:c.667G>T MANE Select	NP_000528.1:p.Val223Phe