Canonical Allele Identifier: CA1234620622

Gene: RPS7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3576488A= , CM000664.2:g.3576488A=	GRCh38
NC_000002.11:g.3624078A= , CM000664.1:g.3624078A=	GRCh37
NC_000002.10:g.3601953A=	NCBI36
NG_011744.1:g.6226A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001011.4:c.149A= MANE Select	NP_001002.1:p.Glu50=
ENST00000645674.2:c.149A= MANE Select	ENSP00000496757.1:p.Glu50=
NM_001011.3:c.149A=	NP_001002.1:p.Glu50=
ENST00000304921.9:c.149A=	ENSP00000339095.4:p.Glu50=
ENST00000403564.5:c.149A=	ENSP00000385018.1:p.Glu50=
ENST00000406376.1:c.149A=	ENSP00000385286.1:p.Glu50=
ENST00000407445.7:c.149A=	ENSP00000385729.3:p.Glu50=
ENST00000407445.8:c.149A=	ENSP00000385729.3:p.Glu50=
ENST00000462576.5:n.434A=
ENST00000479123.1:n.126A=
ENST00000481006.1:n.999A=
ENST00000491937.5:n.414A=
ENST00000491937.6:n.195A=
ENST00000645540.1:n.44-122A=
ENST00000646909.1:c.149A=	ENSP00000496654.1:p.Glu50=
ENST00000647131.1:c.148-71A=	ENSP00000494995.1:n.148-71A=