Canonical Allele Identifier: CA889550516

Gene: RPS27

Linked Data

• dbSNP Id: rs1409988181
• gnomAD v3: 1-153990944-C-T
• gnomAD v4: 1-153990944-C-T
• MyVariant Identifiers: chr1:g.153963420C>T (hg19) ; chr1:g.153990944C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153990944C>T , CM000663.2:g.153990944C>T	GRCh38
NC_000001.10:g.153963420C>T , CM000663.1:g.153963420C>T	GRCh37
NC_000001.9:g.152230044C>T	NCBI36
NG_053102.2:g.5190C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.24C>T
ENST00000643794.1:c.37C>T	ENSP00000495765.1:p.Arg13Trp
ENST00000651669.1:c.6+142C>T MANE Select	ENSP00000499044.1:n.6+142C>T
ENST00000368567.4:c.6+142C>T	ENSP00000357555.4:n.6+142C>T
ENST00000392558.4:c.6+142C>T	ENSP00000376341.4:n.6+142C>T
ENST00000477151.1:n.71C>T
ENST00000493224.5:n.182C>T
NM_001030.4:c.6+142C>T	NP_001021.1:n.6+142C>T
NM_001030.6:c.6+142C>T MANE Select	NP_001021.1:n.6+142C>T
NM_001349946.1:c.-181C>T	NP_001336875.1:n.-181C>T
NM_001349947.1:c.-181C>T	NP_001336876.1:n.-181C>T
NM_001349946.2:c.-181C>T	NP_001336875.1:n.-181C>T
NM_001349947.2:c.-181C>T	NP_001336876.1:n.-181C>T