Canonical Allele Identifier: CA340528

Gene: RPS7

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3575889G>A , CM000664.2:g.3575889G>A	GRCh38
NC_000002.11:g.3623479G>A , CM000664.1:g.3623479G>A	GRCh37
NC_000002.10:g.3601354G>A	NCBI36
NG_011744.1:g.5627G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407445.8:c.147+1G>A	ENSP00000385729.3:n.147+1G>A
ENST00000491937.6:n.193+1G>A
ENST00000645540.1:n.43+1G>A
ENST00000645674.2:c.147+1G>A MANE Select	ENSP00000496757.1:n.147+1G>A
ENST00000646909.1:c.147+1G>A	ENSP00000496654.1:n.147+1G>A
ENST00000647131.1:c.147+1G>A	ENSP00000494995.1:n.147+1G>A
ENST00000304921.9:c.147+1G>A	ENSP00000339095.4:n.147+1G>A
ENST00000403564.5:c.147+1G>A	ENSP00000385018.1:n.147+1G>A
ENST00000406376.1:c.147+1G>A	ENSP00000385286.1:n.147+1G>A
ENST00000407445.7:c.147+1G>A	ENSP00000385729.3:n.147+1G>A
ENST00000462576.5:n.432+1G>A
ENST00000479123.1:n.124+1G>A
ENST00000481006.1:n.400G>A
ENST00000491937.5:n.412+1G>A
NM_001011.3:c.147+1G>A	NP_001002.1:n.147+1G>A
NM_001011.4:c.147+1G>A MANE Select	NP_001002.1:n.147+1G>A