Canonical Allele Identifier: CA1234620170

Gene: RPS7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3575828G= , CM000664.2:g.3575828G=	GRCh38
NC_000002.11:g.3623418G= , CM000664.1:g.3623418G=	GRCh37
NC_000002.10:g.3601293G=	NCBI36
NG_011744.1:g.5566G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000407445.8:c.87G=	ENSP00000385729.3:p.Glu29=
ENST00000491937.6:n.133G=
ENST00000645674.2:c.87G= MANE Select	ENSP00000496757.1:p.Glu29=
ENST00000646909.1:c.87G=	ENSP00000496654.1:p.Glu29=
ENST00000647131.1:c.87G=	ENSP00000494995.1:p.Glu29=
ENST00000304921.9:c.87G=	ENSP00000339095.4:p.Glu29=
ENST00000403564.5:c.87G=	ENSP00000385018.1:p.Glu29=
ENST00000406376.1:c.87G=	ENSP00000385286.1:p.Glu29=
ENST00000407445.7:c.87G=	ENSP00000385729.3:p.Glu29=
ENST00000462576.5:n.372G=
ENST00000479123.1:n.64G=
ENST00000481006.1:n.339G=
ENST00000491937.5:n.352G=
NM_001011.3:c.87G=	NP_001002.1:p.Glu29=
NM_001011.4:c.87G= MANE Select	NP_001002.1:p.Glu29=