Canonical Allele Identifier: CA2038229559

Gene: RPS26

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56042124C= , CM000674.2:g.56042124C=	GRCh38
NC_000012.11:g.56435908C= , CM000674.1:g.56435908C=	GRCh37
NC_000012.10:g.54722175C=	NCBI36
NG_023201.1:g.5223C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-43C=	ENSP00000348849.5:n.-43C=
ENST00000646449.2:c.-43C= MANE Select	ENSP00000496643.1:n.-43C=
ENST00000356464.9:c.-43C=	ENSP00000348849.5:n.-43C=
ENST00000552361.1:c.-34-9C=	ENSP00000450339.1:n.-34-9C=
NM_001029.3:c.-43C=	NP_001020.2:n.-43C=
NM_001029.5:c.-43C= MANE Select	NP_001020.2:n.-43C=