Canonical Allele Identifier: CA2480680465
Gene: RPS27 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153991270G= , CM000663.2:g.153991270G= GRCh38
NC_000001.10:g.153963746G= , CM000663.1:g.153963746G= GRCh37
NC_000001.9:g.152230370G= NCBI36
NG_053102.2:g.5516G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000477151.2:n.303+47G=
ENST00000643794.1:c.236+47G= ENSP00000495765.1:n.236+47G=
ENST00000651669.1:c.115+47G= MANE Select ENSP00000499044.1:n.115+47G=
ENST00000368567.4:c.115+47G= ENSP00000357555.4:n.115+47G=
ENST00000392558.4:c.162G= ENSP00000376341.4:p.Gln54=
ENST00000477151.1:n.270+47G=
ENST00000493224.5:n.381+47G=
NM_001030.4:c.115+47G= NP_001021.1:n.115+47G=
NM_001030.6:c.115+47G= MANE Select NP_001021.1:n.115+47G=
NM_001349946.1:c.19+47G= NP_001336875.1:n.19+47G=
NM_001349947.1:c.19+47G= NP_001336876.1:n.19+47G=
NM_001349946.2:c.19+47G= NP_001336875.1:n.19+47G=
NM_001349947.2:c.19+47G= NP_001336876.1:n.19+47G=
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