Canonical Allele Identifier: CA2575186527

Gene: RPS26

Linked Data

• gnomAD v4: 12-56042122-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56042122G>T , CM000674.2:g.56042122G>T	GRCh38
NC_000012.11:g.56435906G>T , CM000674.1:g.56435906G>T	GRCh37
NC_000012.10:g.54722173G>T	NCBI36
NG_023201.1:g.5221G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-45G>T	ENSP00000348849.5:n.-45G>T
ENST00000646449.2:c.-45G>T MANE Select	ENSP00000496643.1:n.-45G>T
ENST00000356464.9:c.-45G>T	ENSP00000348849.5:n.-45G>T
ENST00000552361.1:c.-34-11G>T	ENSP00000450339.1:n.-34-11G>T
NM_001029.3:c.-45G>T	NP_001020.2:n.-45G>T
NM_001029.5:c.-45G>T MANE Select	NP_001020.2:n.-45G>T