Canonical Allele Identifier: CA342587683

Gene: RPS27

Linked Data

• gnomAD v4: 1-153991197-C-G
• MyVariant Identifiers: chr1:g.153963673C>G (hg19) ; chr1:g.153991197C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991197C>G , CM000663.2:g.153991197C>G	GRCh38
NC_000001.10:g.153963673C>G , CM000663.1:g.153963673C>G	GRCh37
NC_000001.9:g.152230297C>G	NCBI36
NG_053102.2:g.5443C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.277C>G
ENST00000643794.1:c.210C>G	ENSP00000495765.1:p.Phe70Leu
ENST00000651669.1:c.89C>G MANE Select	ENSP00000499044.1:p.Ser30Cys
ENST00000368567.4:c.89C>G	ENSP00000357555.4:p.Ser30Cys
ENST00000392558.4:c.89C>G	ENSP00000376341.4:p.Ser30Cys
ENST00000477151.1:n.244C>G
ENST00000493224.5:n.355C>G
NM_001030.4:c.89C>G	NP_001021.1:p.Ser30Cys
NM_001030.6:c.89C>G MANE Select	NP_001021.1:p.Ser30Cys
NM_001349946.1:c.-8C>G	NP_001336875.1:n.-8C>G
NM_001349947.1:c.-8C>G	NP_001336876.1:n.-8C>G
NM_001349946.2:c.-8C>G	NP_001336875.1:n.-8C>G
NM_001349947.2:c.-8C>G	NP_001336876.1:n.-8C>G