Canonical Allele Identifier: CA420949201
Gene: RPS27 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.153963677C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153991201C>T , CM000663.2:g.153991201C>T GRCh38
NC_000001.10:g.153963677C>T , CM000663.1:g.153963677C>T GRCh37
NC_000001.9:g.152230301C>T NCBI36
NG_053102.2:g.5447C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000477151.2:n.281C>T
ENST00000643794.1:c.214C>T ENSP00000495765.1:p.Leu72Phe
ENST00000651669.1:c.93C>T MANE Select ENSP00000499044.1:p.Tyr31=
ENST00000368567.4:c.93C>T ENSP00000357555.4:p.Tyr31=
ENST00000392558.4:c.93C>T ENSP00000376341.4:p.Tyr31=
ENST00000477151.1:n.248C>T
ENST00000493224.5:n.359C>T
NM_001030.4:c.93C>T NP_001021.1:p.Tyr31=
NM_001030.6:c.93C>T MANE Select NP_001021.1:p.Tyr31=
NM_001349946.1:c.-4C>T NP_001336875.1:n.-4C>T
NM_001349947.1:c.-4C>T NP_001336876.1:n.-4C>T
NM_001349946.2:c.-4C>T NP_001336875.1:n.-4C>T
NM_001349947.2:c.-4C>T NP_001336876.1:n.-4C>T