Canonical Allele Identifier: CA2480680436
Gene: RPS27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153991198C= , CM000663.2:g.153991198C= GRCh38
NC_000001.10:g.153963674C= , CM000663.1:g.153963674C= GRCh37
NC_000001.9:g.152230298C= NCBI36
NG_053102.2:g.5444C=

Transcript Alleles

HGVS Amino-acid change
ENST00000477151.2:n.278C=
ENST00000643794.1:c.211C= ENSP00000495765.1:p.Leu71=
ENST00000651669.1:c.90C= MANE Select ENSP00000499044.1:p.Ser30=
ENST00000368567.4:c.90C= ENSP00000357555.4:p.Ser30=
ENST00000392558.4:c.90C= ENSP00000376341.4:p.Ser30=
ENST00000477151.1:n.245C=
ENST00000493224.5:n.356C=
NM_001030.4:c.90C= NP_001021.1:p.Ser30=
NM_001030.6:c.90C= MANE Select NP_001021.1:p.Ser30=
NM_001349946.1:c.-7C= NP_001336875.1:n.-7C=
NM_001349947.1:c.-7C= NP_001336876.1:n.-7C=
NM_001349946.2:c.-7C= NP_001336875.1:n.-7C=
NM_001349947.2:c.-7C= NP_001336876.1:n.-7C=