Canonical Allele Identifier: CA646075998

Gene: RPS27

Linked Data

• COSMIC: COSN5026226 ; COSN5026227

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153990764T>G , CM000663.2:g.153990764T>G	GRCh38
NC_000001.10:g.153963240T>G , CM000663.1:g.153963240T>G	GRCh37
NC_000001.9:g.152229864T>G	NCBI36
NG_053102.2:g.5010T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643794.1:c.-33T>G	ENSP00000495765.1:n.-33T>G
ENST00000651669.1:c.-33T>G MANE Select	ENSP00000499044.1:n.-33T>G
ENST00000368567.4:c.-33T>G	ENSP00000357555.4:n.-33T>G
ENST00000392558.4:c.-33T>G	ENSP00000376341.4:n.-33T>G
ENST00000477151.1:n.2T>G
ENST00000493224.5:n.2T>G
NM_001030.4:c.-33T>G	NP_001021.1:n.-33T>G
NM_001030.6:c.-33T>G MANE Select	NP_001021.1:n.-33T>G
NM_001349946.1:c.-250T>G	NP_001336875.1:n.-250T>G
NM_001349947.1:c.-361T>G	NP_001336876.1:n.-361T>G
NM_001349946.2:c.-250T>G	NP_001336875.1:n.-250T>G
NM_001349947.2:c.-361T>G	NP_001336876.1:n.-361T>G