Canonical Allele Identifier: CA420866981

Gene: RPS27

Linked Data

• gnomAD v4: 1-153991129-C-G
• MyVariant Identifiers: chr1:g.153963605C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991129C>G , CM000663.2:g.153991129C>G	GRCh38
NC_000001.10:g.153963605C>G , CM000663.1:g.153963605C>G	GRCh37
NC_000001.9:g.152230229C>G	NCBI36
NG_053102.2:g.5375C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.209C>G
ENST00000643794.1:c.142C>G	ENSP00000495765.1:p.Pro48Ala
ENST00000651669.1:c.21C>G MANE Select	ENSP00000499044.1:p.Leu7=
ENST00000368567.4:c.21C>G	ENSP00000357555.4:p.Leu7=
ENST00000392558.4:c.21C>G	ENSP00000376341.4:p.Leu7=
ENST00000477151.1:n.176C>G
ENST00000493224.5:n.287C>G
NM_001030.4:c.21C>G	NP_001021.1:p.Leu7=
NM_001030.6:c.21C>G MANE Select	NP_001021.1:p.Leu7=
NM_001349946.1:c.-76C>G	NP_001336875.1:n.-76C>G
NM_001349947.1:c.-76C>G	NP_001336876.1:n.-76C>G
NM_001349946.2:c.-76C>G	NP_001336875.1:n.-76C>G
NM_001349947.2:c.-76C>G	NP_001336876.1:n.-76C>G