Canonical Allele Identifier: CA41546686
Gene: RPS7 HGNC NCBI

Linked Data

dbSNP Id: rs116840810

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000407445.8:c.149A>G ENSP00000385729.3:p.Glu50Gly
ENST00000491937.6:n.195A>G
ENST00000645540.1:n.44-122A>G
ENST00000645674.2:c.149A>G MANE Select ENSP00000496757.1:p.Glu50Gly
ENST00000646909.1:c.149A>G ENSP00000496654.1:p.Glu50Gly
ENST00000647131.1:c.148-71A>G ENSP00000494995.1:n.148-71A>G
ENST00000304921.9:c.149A>G ENSP00000339095.4:p.Glu50Gly
ENST00000403564.5:c.149A>G ENSP00000385018.1:p.Glu50Gly
ENST00000406376.1:c.149A>G ENSP00000385286.1:p.Glu50Gly
ENST00000407445.7:c.149A>G ENSP00000385729.3:p.Glu50Gly
ENST00000462576.5:n.434A>G
ENST00000479123.1:n.126A>G
ENST00000481006.1:n.999A>G
ENST00000491937.5:n.414A>G
NM_001011.3:c.149A>G NP_001002.1:p.Glu50Gly
NM_001011.4:c.149A>G MANE Select NP_001002.1:p.Glu50Gly