Canonical Allele Identifier: CA2648113997

Gene: RPS27

Linked Data

• gnomAD v4: 1-153991006-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991006C>A , CM000663.2:g.153991006C>A	GRCh38
NC_000001.10:g.153963482C>A , CM000663.1:g.153963482C>A	GRCh37
NC_000001.9:g.152230106C>A	NCBI36
NG_053102.2:g.5252C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.86C>A
ENST00000643794.1:c.99C>A	ENSP00000495765.1:p.Thr33=
ENST00000651669.1:c.7-109C>A MANE Select	ENSP00000499044.1:n.7-109C>A
ENST00000368567.4:c.7-109C>A	ENSP00000357555.4:n.7-109C>A
ENST00000392558.4:c.7-109C>A	ENSP00000376341.4:n.7-109C>A
ENST00000477151.1:n.133C>A
ENST00000493224.5:n.244C>A
NM_001030.4:c.7-109C>A	NP_001021.1:n.7-109C>A
NM_001030.6:c.7-109C>A MANE Select	NP_001021.1:n.7-109C>A
NM_001349946.1:c.-119C>A	NP_001336875.1:n.-119C>A
NM_001349947.1:c.-119C>A	NP_001336876.1:n.-119C>A
NM_001349946.2:c.-119C>A	NP_001336875.1:n.-119C>A
NM_001349947.2:c.-119C>A	NP_001336876.1:n.-119C>A