Canonical Allele Identifier: CA342587691
Gene: RPS27 HGNC NCBI

Linked Data

gnomAD v4: 1-153991201-C-A
MyVariant Identifiers: chr1:g.153963677C>A (hg19) chr1:g.153991201C>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000477151.2:n.281C>A
ENST00000643794.1:c.214C>A ENSP00000495765.1:p.Leu72Ile
ENST00000651669.1:c.93C>A MANE Select ENSP00000499044.1:p.Tyr31Ter
ENST00000368567.4:c.93C>A ENSP00000357555.4:p.Tyr31Ter
ENST00000392558.4:c.93C>A ENSP00000376341.4:p.Tyr31Ter
ENST00000477151.1:n.248C>A
ENST00000493224.5:n.359C>A
NM_001030.4:c.93C>A NP_001021.1:p.Tyr31Ter
NM_001030.6:c.93C>A MANE Select NP_001021.1:p.Tyr31Ter
NM_001349946.1:c.-4C>A NP_001336875.1:n.-4C>A
NM_001349947.1:c.-4C>A NP_001336876.1:n.-4C>A
NM_001349946.2:c.-4C>A NP_001336875.1:n.-4C>A
NM_001349947.2:c.-4C>A NP_001336876.1:n.-4C>A
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