Canonical Allele Identifier: CA420949194
Gene: RPS27 HGNC NCBI

Linked Data

gnomAD v4: 1-153991198-C-A
MyVariant Identifiers: chr1:g.153963674C>A (hg19)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000477151.2:n.278C>A
ENST00000643794.1:c.211C>A ENSP00000495765.1:p.Leu71Ile
ENST00000651669.1:c.90C>A MANE Select ENSP00000499044.1:p.Ser30=
ENST00000368567.4:c.90C>A ENSP00000357555.4:p.Ser30=
ENST00000392558.4:c.90C>A ENSP00000376341.4:p.Ser30=
ENST00000477151.1:n.245C>A
ENST00000493224.5:n.356C>A
NM_001030.4:c.90C>A NP_001021.1:p.Ser30=
NM_001030.6:c.90C>A MANE Select NP_001021.1:p.Ser30=
NM_001349946.1:c.-7C>A NP_001336875.1:n.-7C>A
NM_001349947.1:c.-7C>A NP_001336876.1:n.-7C>A
NM_001349946.2:c.-7C>A NP_001336875.1:n.-7C>A
NM_001349947.2:c.-7C>A NP_001336876.1:n.-7C>A
Search 100 bp 5'
Search 100 bp 3'