Canonical Allele Identifier: CA2501167492

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991107_153991108insTT , CM000663.2:g.153991107_153991108insTT	GRCh38
NC_000001.10:g.153963583_153963584insTT , CM000663.1:g.153963583_153963584insTT	GRCh37
NC_000001.9:g.152230207_152230208insTT	NCBI36
NG_053102.2:g.5353_5354insTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000477151.2:n.187_188insTT
ENST00000643794.1:c.128-8_128-7insTT	ENSP00000495765.1:n.128-8_128-7insTT
ENST00000651669.1:c.7-8_7-7insTT MANE Select	ENSP00000499044.1:n.7-8_7-7insTT
ENST00000368567.4:c.7-8_7-7insTT	ENSP00000357555.4:n.7-8_7-7insTT
ENST00000392558.4:c.7-8_7-7insTT	ENSP00000376341.4:n.7-8_7-7insTT
ENST00000477151.1:n.162-8_162-7insTT
ENST00000493224.5:n.273-8_273-7insTT
NM_001030.4:c.7-8_7-7insTT	NP_001021.1:n.7-8_7-7insTT
NM_001030.6:c.7-8_7-7insTT MANE Select	NP_001021.1:n.7-8_7-7insTT
NM_001349946.1:c.-90-8_-90-7insTT	NP_001336875.1:n.-90-8_-90-7insTT
NM_001349947.1:c.-90-8_-90-7insTT	NP_001336876.1:n.-90-8_-90-7insTT
NM_001349946.2:c.-90-8_-90-7insTT	NP_001336875.1:n.-90-8_-90-7insTT
NM_001349947.2:c.-90-8_-90-7insTT	NP_001336876.1:n.-90-8_-90-7insTT