Canonical Allele Identifier: CA915943693

Gene: RPS7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3580802T>G , CM000664.2:g.3580802T>G	GRCh38
NC_000002.11:g.3628392T>G , CM000664.1:g.3628392T>G	GRCh37
NC_000002.10:g.3606267T>G	NCBI36
NG_011744.1:g.10540T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001011.4:c.508-3T>G MANE Select	NP_001002.1:n.508-3T>G
ENST00000645674.2:c.508-3T>G MANE Select	ENSP00000496757.1:n.508-3T>G
NM_001011.3:c.508-3T>G	NP_001002.1:n.508-3T>G
ENST00000304921.9:c.508-3T>G	ENSP00000339095.4:n.508-3T>G
ENST00000403564.5:c.508-3T>G	ENSP00000385018.1:n.508-3T>G
ENST00000406376.1:c.508-3T>G	ENSP00000385286.1:n.508-3T>G
ENST00000462576.5:n.793-3T>G
ENST00000472966.1:n.443-3T>G
ENST00000481006.1:n.5313T>G
ENST00000645540.1:n.281-3T>G
ENST00000646909.1:c.508-3T>G	ENSP00000496654.1:n.508-3T>G
ENST00000647131.1:c.436-3T>G	ENSP00000494995.1:n.436-3T>G