Canonical Allele Identifier: CA41546186

Gene: RPS7

Linked Data

• dbSNP Id: rs201230139
• gnomAD v4: 2-3575828-G-A
• MyVariant Identifiers: chr2:g.3623418G>A (hg19) ; chr2:g.3575828G>A (hg38)

Genomic Alleles

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

Transcript Alleles

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