Canonical Allele Identifier: CA342587696

Gene: RPS27

Linked Data

• dbSNP Id: rs1424373971
• gnomAD v2: 1-153963679-T-A
• gnomAD v4: 1-153991203-T-A
• MyVariant Identifiers: chr1:g.153963679T>A (hg19) ; chr1:g.153991203T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991203T>A , CM000663.2:g.153991203T>A	GRCh38
NC_000001.10:g.153963679T>A , CM000663.1:g.153963679T>A	GRCh37
NC_000001.9:g.152230303T>A	NCBI36
NG_053102.2:g.5449T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000477151.2:n.283T>A
ENST00000643794.1:c.216T>A	ENSP00000495765.1:p.Leu72=
ENST00000651669.1:c.95T>A MANE Select	ENSP00000499044.1:p.Phe32Tyr
ENST00000368567.4:c.95T>A	ENSP00000357555.4:p.Phe32Tyr
ENST00000392558.4:c.95T>A	ENSP00000376341.4:p.Phe32Tyr
ENST00000477151.1:n.250T>A
ENST00000493224.5:n.361T>A
NM_001030.4:c.95T>A	NP_001021.1:p.Phe32Tyr
NM_001030.6:c.95T>A MANE Select	NP_001021.1:p.Phe32Tyr
NM_001349946.1:c.-2T>A	NP_001336875.1:n.-2T>A
NM_001349947.1:c.-2T>A	NP_001336876.1:n.-2T>A
NM_001349946.2:c.-2T>A	NP_001336875.1:n.-2T>A
NM_001349947.2:c.-2T>A	NP_001336876.1:n.-2T>A