Canonical Allele Identifier: CA2659094258

Gene: RPS27A

Linked Data

• gnomAD v4: 2-55234222-GCAGCCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55234224_55234229del , CM000664.2:g.55234224_55234229del	GRCh38
NC_000002.11:g.55461360_55461365del , CM000664.1:g.55461360_55461365del	GRCh37
NC_000002.10:g.55314864_55314869del	NCBI36
NG_017017.1:g.7296_7301del
NG_033063.1:g.3336_3341del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272317.11:c.189+20_189+25del MANE Select	ENSP00000272317.6:n.189+20_189+25del
ENST00000272317.10:c.189+20_189+25del	ENSP00000272317.6:n.189+20_189+25del
ENST00000402285.7:c.189+20_189+25del	ENSP00000383981.3:n.189+20_189+25del
ENST00000404735.1:c.189+20_189+25del	ENSP00000385659.1:n.189+20_189+25del
ENST00000449323.5:c.189+20_189+25del	ENSP00000408482.1:n.189+20_189+25del
ENST00000468810.1:n.167_172del
ENST00000478196.6:n.226+20_226+25del
ENST00000495843.1:n.239_244del
NM_001135592.2:c.189+20_189+25del	NP_001129064.1:n.189+20_189+25del
NM_001177413.1:c.189+20_189+25del	NP_001170884.1:n.189+20_189+25del
NM_002954.5:c.189+20_189+25del	NP_002945.1:n.189+20_189+25del
NM_002954.6:c.189+20_189+25del MANE Select	NP_002945.1:n.189+20_189+25del