Canonical Allele Identifier: CA342587733

Gene: RPS27

Linked Data

• gnomAD v4: 1-153991217-T-G
• MyVariant Identifiers: chr1:g.153963693T>G (hg19) ; chr1:g.153991217T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991217T>G , CM000663.2:g.153991217T>G	GRCh38
NC_000001.10:g.153963693T>G , CM000663.1:g.153963693T>G	GRCh37
NC_000001.9:g.152230317T>G	NCBI36
NG_053102.2:g.5463T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.297T>G
ENST00000643794.1:c.230T>G	ENSP00000495765.1:p.Met77Arg
ENST00000651669.1:c.109T>G MANE Select	ENSP00000499044.1:p.Cys37Gly
ENST00000368567.4:c.109T>G	ENSP00000357555.4:p.Cys37Gly
ENST00000392558.4:c.109T>G	ENSP00000376341.4:p.Cys37Gly
ENST00000477151.1:n.264T>G
ENST00000493224.5:n.375T>G
NM_001030.4:c.109T>G	NP_001021.1:p.Cys37Gly
NM_001030.6:c.109T>G MANE Select	NP_001021.1:p.Cys37Gly
NM_001349946.1:c.13T>G	NP_001336875.1:p.Cys5Gly
NM_001349947.1:c.13T>G	NP_001336876.1:p.Cys5Gly
NM_001349946.2:c.13T>G	NP_001336875.1:p.Cys5Gly
NM_001349947.2:c.13T>G	NP_001336876.1:p.Cys5Gly