Canonical Allele Identifier: CA342587708
Gene: RPS27 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.153963683G>C (hg19) chr1:g.153991207G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153991207G>C , CM000663.2:g.153991207G>C GRCh38
NC_000001.10:g.153963683G>C , CM000663.1:g.153963683G>C GRCh37
NC_000001.9:g.152230307G>C NCBI36
NG_053102.2:g.5453G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000477151.2:n.287G>C
ENST00000643794.1:c.220G>C ENSP00000495765.1:p.Gly74Arg
ENST00000651669.1:c.99G>C MANE Select ENSP00000499044.1:p.Met33Ile
ENST00000368567.4:c.99G>C ENSP00000357555.4:p.Met33Ile
ENST00000392558.4:c.99G>C ENSP00000376341.4:p.Met33Ile
ENST00000477151.1:n.254G>C
ENST00000493224.5:n.365G>C
NM_001030.4:c.99G>C NP_001021.1:p.Met33Ile
NM_001030.6:c.99G>C MANE Select NP_001021.1:p.Met33Ile
NM_001349946.1:c.3G>C NP_001336875.1:p.Met1Ile
NM_001349947.1:c.3G>C NP_001336876.1:p.Met1Ile
NM_001349946.2:c.3G>C NP_001336875.1:p.Met1Ile
NM_001349947.2:c.3G>C NP_001336876.1:p.Met1Ile
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