Canonical Allele Identifier: CA342587717

Gene: RPS27

Linked Data

• MyVariant Identifiers: chr1:g.153963687G>A (hg19) ; chr1:g.153991211G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991211G>A , CM000663.2:g.153991211G>A	GRCh38
NC_000001.10:g.153963687G>A , CM000663.1:g.153963687G>A	GRCh37
NC_000001.9:g.152230311G>A	NCBI36
NG_053102.2:g.5457G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000477151.2:n.291G>A
ENST00000643794.1:c.224G>A	ENSP00000495765.1:p.Cys75Tyr
ENST00000651669.1:c.103G>A MANE Select	ENSP00000499044.1:p.Val35Met
ENST00000368567.4:c.103G>A	ENSP00000357555.4:p.Val35Met
ENST00000392558.4:c.103G>A	ENSP00000376341.4:p.Val35Met
ENST00000477151.1:n.258G>A
ENST00000493224.5:n.369G>A
NM_001030.4:c.103G>A	NP_001021.1:p.Val35Met
NM_001030.6:c.103G>A MANE Select	NP_001021.1:p.Val35Met
NM_001349946.1:c.7G>A	NP_001336875.1:p.Val3Met
NM_001349947.1:c.7G>A	NP_001336876.1:p.Val3Met
NM_001349946.2:c.7G>A	NP_001336875.1:p.Val3Met
NM_001349947.2:c.7G>A	NP_001336876.1:p.Val3Met