Canonical Allele Identifier: CA2038229514

Gene: RPS26

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56042071C= , CM000674.2:g.56042071C=	GRCh38
NC_000012.11:g.56435855C= , CM000674.1:g.56435855C=	GRCh37
NC_000012.10:g.54722122C=	NCBI36
NG_023201.1:g.5170C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-96C=	ENSP00000348849.5:n.-96C=
ENST00000646449.2:c.-96C= MANE Select	ENSP00000496643.1:n.-96C=
ENST00000356464.9:c.-96C=	ENSP00000348849.5:n.-96C=
ENST00000552361.1:c.-35+7C=	ENSP00000450339.1:n.-35+7C=
NM_001029.3:c.-96C=	NP_001020.2:n.-96C=
NM_001029.5:c.-96C= MANE Select	NP_001020.2:n.-96C=