Canonical Allele Identifier: CA1123876

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991521_153991522dup , CM000663.2:g.153991521_153991522dup	GRCh38
NC_000001.10:g.153963997_153963998dup , CM000663.1:g.153963997_153963998dup	GRCh37
NC_000001.9:g.152230621_152230622dup	NCBI36
NG_053102.2:g.5767_5768dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.304-45_304-44dup
ENST00000643794.1:c.237-45_237-44dup	ENSP00000495765.1:n.237-45_237-44dup
ENST00000651669.1:c.116-45_116-44dup MANE Select	ENSP00000499044.1:n.116-45_116-44dup
ENST00000368567.4:c.116-45_116-44dup	ENSP00000357555.4:n.116-45_116-44dup
ENST00000392558.4:c.*212_*213dup	ENSP00000376341.4:n.*212_*213dup
ENST00000477151.1:n.271-45_271-44dup
ENST00000493224.5:n.382-45_382-44dup
NM_001030.4:c.116-45_116-44dup	NP_001021.1:n.116-45_116-44dup
NM_001030.6:c.116-45_116-44dup MANE Select	NP_001021.1:n.116-45_116-44dup
NM_001349946.1:c.20-45_20-44dup	NP_001336875.1:n.20-45_20-44dup
NM_001349947.1:c.20-45_20-44dup	NP_001336876.1:n.20-45_20-44dup
NM_001349946.2:c.20-45_20-44dup	NP_001336875.1:n.20-45_20-44dup
NM_001349947.2:c.20-45_20-44dup	NP_001336876.1:n.20-45_20-44dup