Canonical Allele Identifier: CA2569908415

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991104_153991105del , CM000663.2:g.153991104_153991105del	GRCh38
NC_000001.10:g.153963580_153963581del , CM000663.1:g.153963580_153963581del	GRCh37
NC_000001.9:g.152230204_152230205del	NCBI36
NG_053102.2:g.5350_5351del

Transcript Alleles

HGVS	Amino-acid change
ENST00000477151.2:n.184_185del
ENST00000643794.1:c.128-11_128-10del	ENSP00000495765.1:n.128-11_128-10del
ENST00000651669.1:c.7-11_7-10del MANE Select	ENSP00000499044.1:n.7-11_7-10del
ENST00000368567.4:c.7-11_7-10del	ENSP00000357555.4:n.7-11_7-10del
ENST00000392558.4:c.7-11_7-10del	ENSP00000376341.4:n.7-11_7-10del
ENST00000477151.1:n.162-11_162-10del
ENST00000493224.5:n.273-11_273-10del
NM_001030.4:c.7-11_7-10del	NP_001021.1:n.7-11_7-10del
NM_001030.6:c.7-11_7-10del MANE Select	NP_001021.1:n.7-11_7-10del
NM_001349946.1:c.-90-11_-90-10del	NP_001336875.1:n.-90-11_-90-10del
NM_001349947.1:c.-90-11_-90-10del	NP_001336876.1:n.-90-11_-90-10del
NM_001349946.2:c.-90-11_-90-10del	NP_001336875.1:n.-90-11_-90-10del
NM_001349947.2:c.-90-11_-90-10del	NP_001336876.1:n.-90-11_-90-10del