Canonical Allele Identifier: CA1252173863

Gene: RPS27A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55234241_55234244delinsAAAT , CM000664.2:g.55234241_55234244delinsAAAT	GRCh38
NC_000002.11:g.55461377_55461380delinsAAAT , CM000664.1:g.55461377_55461380delinsAAAT	GRCh37
NC_000002.10:g.55314881_55314884delinsAAAT	NCBI36
NG_017017.1:g.7313_7316delinsAAAT
NG_033063.1:g.3320_3323delinsATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272317.11:c.189+37_189+40delinsAAAT MANE Select	ENSP00000272317.6:n.189+37_189+40delinsAAAT
ENST00000272317.10:c.189+37_189+40delinsAAAT	ENSP00000272317.6:n.189+37_189+40delinsAAAT
ENST00000402285.7:c.189+37_189+40delinsAAAT	ENSP00000383981.3:n.189+37_189+40delinsAAAT
ENST00000404735.1:c.189+37_189+40delinsAAAT	ENSP00000385659.1:n.189+37_189+40delinsAAAT
ENST00000449323.5:c.189+37_189+40delinsAAAT	ENSP00000408482.1:n.189+37_189+40delinsAAAT
ENST00000468810.1:n.184_187delinsAAAT
ENST00000478196.6:n.226+37_226+40delinsAAAT
ENST00000495843.1:n.256_259delinsAAAT
NM_001135592.2:c.189+37_189+40delinsAAAT	NP_001129064.1:n.189+37_189+40delinsAAAT
NM_001177413.1:c.189+37_189+40delinsAAAT	NP_001170884.1:n.189+37_189+40delinsAAAT
NM_002954.5:c.189+37_189+40delinsAAAT	NP_002945.1:n.189+37_189+40delinsAAAT
NM_002954.6:c.189+37_189+40delinsAAAT MANE Select	NP_002945.1:n.189+37_189+40delinsAAAT