Canonical Allele Identifier: CA2480680404
Gene: RPS27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153991110C= , CM000663.2:g.153991110C= GRCh38
NC_000001.10:g.153963586C= , CM000663.1:g.153963586C= GRCh37
NC_000001.9:g.152230210C= NCBI36
NG_053102.2:g.5356C=

Transcript Alleles

HGVS Amino-acid change
ENST00000477151.2:n.190C=
ENST00000643794.1:c.128-5C= ENSP00000495765.1:n.128-5C=
ENST00000651669.1:c.7-5C= MANE Select ENSP00000499044.1:n.7-5C=
ENST00000368567.4:c.7-5C= ENSP00000357555.4:n.7-5C=
ENST00000392558.4:c.7-5C= ENSP00000376341.4:n.7-5C=
ENST00000477151.1:n.162-5C=
ENST00000493224.5:n.273-5C=
NM_001030.4:c.7-5C= NP_001021.1:n.7-5C=
NM_001030.6:c.7-5C= MANE Select NP_001021.1:n.7-5C=
NM_001349946.1:c.-90-5C= NP_001336875.1:n.-90-5C=
NM_001349947.1:c.-90-5C= NP_001336876.1:n.-90-5C=
NM_001349946.2:c.-90-5C= NP_001336875.1:n.-90-5C=
NM_001349947.2:c.-90-5C= NP_001336876.1:n.-90-5C=