Canonical Allele Identifier: CA1140474980
Gene: RPS27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153991208G= , CM000663.2:g.153991208G= GRCh38
NC_000001.10:g.153963684G= , CM000663.1:g.153963684G= GRCh37
NC_000001.9:g.152230308G= NCBI36
NG_053102.2:g.5454G=

Transcript Alleles

HGVS Amino-acid change
ENST00000477151.2:n.288G=
ENST00000643794.1:c.221G= ENSP00000495765.1:p.Gly74=
ENST00000651669.1:c.100G= MANE Select ENSP00000499044.1:p.Asp34=
ENST00000368567.4:c.100G= ENSP00000357555.4:p.Asp34=
ENST00000392558.4:c.100G= ENSP00000376341.4:p.Asp34=
ENST00000477151.1:n.255G=
ENST00000493224.5:n.366G=
NM_001030.4:c.100G= NP_001021.1:p.Asp34=
NM_001030.6:c.100G= MANE Select NP_001021.1:p.Asp34=
NM_001349946.1:c.4G= NP_001336875.1:p.Asp2=
NM_001349947.1:c.4G= NP_001336876.1:p.Asp2=
NM_001349946.2:c.4G= NP_001336875.1:p.Asp2=
NM_001349947.2:c.4G= NP_001336876.1:p.Asp2=