Canonical Allele Identifier: CA1252173864

Gene: RPS27A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55234242_55234244delinsAAT , CM000664.2:g.55234242_55234244delinsAAT	GRCh38
NC_000002.11:g.55461378_55461380delinsAAT , CM000664.1:g.55461378_55461380delinsAAT	GRCh37
NC_000002.10:g.55314882_55314884delinsAAT	NCBI36
NG_017017.1:g.7314_7316delinsAAT
NG_033063.1:g.3320_3322delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272317.11:c.189+38_189+40delinsAAT MANE Select	ENSP00000272317.6:n.189+38_189+40delinsAAT
ENST00000272317.10:c.189+38_189+40delinsAAT	ENSP00000272317.6:n.189+38_189+40delinsAAT
ENST00000402285.7:c.189+38_189+40delinsAAT	ENSP00000383981.3:n.189+38_189+40delinsAAT
ENST00000404735.1:c.189+38_189+40delinsAAT	ENSP00000385659.1:n.189+38_189+40delinsAAT
ENST00000449323.5:c.189+38_189+40delinsAAT	ENSP00000408482.1:n.189+38_189+40delinsAAT
ENST00000468810.1:n.185_187delinsAAT
ENST00000478196.6:n.226+38_226+40delinsAAT
ENST00000495843.1:n.257_259delinsAAT
NM_001135592.2:c.189+38_189+40delinsAAT	NP_001129064.1:n.189+38_189+40delinsAAT
NM_001177413.1:c.189+38_189+40delinsAAT	NP_001170884.1:n.189+38_189+40delinsAAT
NM_002954.5:c.189+38_189+40delinsAAT	NP_002945.1:n.189+38_189+40delinsAAT
NM_002954.6:c.189+38_189+40delinsAAT MANE Select	NP_002945.1:n.189+38_189+40delinsAAT