Canonical Allele Identifier: CA1139656747

Gene: RPS7

Linked Data

• ClinVar Variation Id: 975849
• ClinVar RCV Id: RCV001252962
• dbSNP Id: rs1064796859

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3575351G>A , CM000664.2:g.3575351G>A	GRCh38
NC_000002.11:g.3622941G>A , CM000664.1:g.3622941G>A	GRCh37
NC_000002.10:g.3600816G>A	NCBI36
NG_011744.1:g.5089G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407445.8:c.-259G>A	ENSP00000385729.3:n.-259G>A
ENST00000491937.6:n.28+1G>A
ENST00000645674.2:c.-19+1G>A MANE Select	ENSP00000496757.1:n.-19+1G>A
ENST00000646909.1:c.-54+1G>A	ENSP00000496654.1:n.-54+1G>A
ENST00000647131.1:c.-19+1G>A	ENSP00000494995.1:n.-19+1G>A
ENST00000304921.9:c.-19+1G>A	ENSP00000339095.4:n.-19+1G>A
ENST00000403564.5:c.-116G>A	ENSP00000385018.1:n.-116G>A
ENST00000407445.7:c.-19+1G>A	ENSP00000385729.3:n.-19+1G>A
ENST00000462576.5:n.27G>A
ENST00000491937.5:n.7G>A
NM_001011.3:c.-19+1G>A	NP_001002.1:n.-19+1G>A
NM_001011.4:c.-19+1G>A MANE Select	NP_001002.1:n.-19+1G>A