Canonical Allele Identifier: CA646075996

Gene: RPS27

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153990766dup , CM000663.2:g.153990766dup	GRCh38
NC_000001.10:g.153963242dup , CM000663.1:g.153963242dup	GRCh37
NC_000001.9:g.152229866dup	NCBI36
NG_053102.2:g.5012dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643794.1:c.-31dup	ENSP00000495765.1:n.-31dup
ENST00000651669.1:c.-31dup MANE Select	ENSP00000499044.1:n.-31dup
ENST00000368567.4:c.-31dup	ENSP00000357555.4:n.-31dup
ENST00000392558.4:c.-31dup	ENSP00000376341.4:n.-31dup
ENST00000477151.1:n.4dup
ENST00000493224.5:n.4dup
NM_001030.4:c.-31dup	NP_001021.1:n.-31dup
NM_001030.6:c.-31dup MANE Select	NP_001021.1:n.-31dup
NM_001349946.1:c.-248dup	NP_001336875.1:n.-248dup
NM_001349947.1:c.-359dup	NP_001336876.1:n.-359dup
NM_001349946.2:c.-248dup	NP_001336875.1:n.-248dup
NM_001349947.2:c.-359dup	NP_001336876.1:n.-359dup