Canonical Allele Identifier: CA2648113923

Gene: RPS27

Linked Data

• gnomAD v4: 1-153990950-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153990950A>C , CM000663.2:g.153990950A>C	GRCh38
NC_000001.10:g.153963426A>C , CM000663.1:g.153963426A>C	GRCh37
NC_000001.9:g.152230050A>C	NCBI36
NG_053102.2:g.5196A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.30A>C
ENST00000643794.1:c.43A>C	ENSP00000495765.1:p.Thr15Pro
ENST00000651669.1:c.6+148A>C MANE Select	ENSP00000499044.1:n.6+148A>C
ENST00000368567.4:c.6+148A>C	ENSP00000357555.4:n.6+148A>C
ENST00000392558.4:c.6+148A>C	ENSP00000376341.4:n.6+148A>C
ENST00000477151.1:n.77A>C
ENST00000493224.5:n.188A>C
NM_001030.4:c.6+148A>C	NP_001021.1:n.6+148A>C
NM_001030.6:c.6+148A>C MANE Select	NP_001021.1:n.6+148A>C
NM_001349946.1:c.-175A>C	NP_001336875.1:n.-175A>C
NM_001349947.1:c.-175A>C	NP_001336876.1:n.-175A>C
NM_001349946.2:c.-175A>C	NP_001336875.1:n.-175A>C
NM_001349947.2:c.-175A>C	NP_001336876.1:n.-175A>C