Canonical Allele Identifier: CA342587718
Gene: RPS27 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.153963687G>C (hg19) chr1:g.153991211G>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000477151.2:n.291G>C
ENST00000643794.1:c.224G>C ENSP00000495765.1:p.Cys75Ser
ENST00000651669.1:c.103G>C MANE Select ENSP00000499044.1:p.Val35Leu
ENST00000368567.4:c.103G>C ENSP00000357555.4:p.Val35Leu
ENST00000392558.4:c.103G>C ENSP00000376341.4:p.Val35Leu
ENST00000477151.1:n.258G>C
ENST00000493224.5:n.369G>C
NM_001030.4:c.103G>C NP_001021.1:p.Val35Leu
NM_001030.6:c.103G>C MANE Select NP_001021.1:p.Val35Leu
NM_001349946.1:c.7G>C NP_001336875.1:p.Val3Leu
NM_001349947.1:c.7G>C NP_001336876.1:p.Val3Leu
NM_001349946.2:c.7G>C NP_001336875.1:p.Val3Leu
NM_001349947.2:c.7G>C NP_001336876.1:p.Val3Leu
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