Canonical Allele Identifier: CA2038229738

Gene: RPS26

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56042170G= , CM000674.2:g.56042170G=	GRCh38
NC_000012.11:g.56435954G= , CM000674.1:g.56435954G=	GRCh37
NC_000012.10:g.54722221G=	NCBI36
NG_023201.1:g.5269G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.3+1G=	ENSP00000348849.5:n.3+1G=
ENST00000646449.2:c.3+1G= MANE Select	ENSP00000496643.1:n.3+1G=
ENST00000356464.9:c.3+1G=	ENSP00000348849.5:n.3+1G=
ENST00000548590.1:n.30+1G=
ENST00000552361.1:c.3+1G=	ENSP00000450339.1:n.3+1G=
NM_001029.3:c.3+1G=	NP_001020.2:n.3+1G=
NM_001029.5:c.3+1G= MANE Select	NP_001020.2:n.3+1G=