Canonical Allele Identifier: CA2659094281

Gene: RPS27A

Linked Data

• gnomAD v4: 2-55234257-ATTTTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55234259_55234263del , CM000664.2:g.55234259_55234263del	GRCh38
NC_000002.11:g.55461395_55461399del , CM000664.1:g.55461395_55461399del	GRCh37
NC_000002.10:g.55314899_55314903del	NCBI36
NG_017017.1:g.7331_7335del
NG_033063.1:g.3302_3306del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272317.11:c.189+55_189+59del MANE Select	ENSP00000272317.6:n.189+55_189+59del
ENST00000272317.10:c.189+55_189+59del	ENSP00000272317.6:n.189+55_189+59del
ENST00000402285.7:c.189+55_189+59del	ENSP00000383981.3:n.189+55_189+59del
ENST00000404735.1:c.189+55_189+59del	ENSP00000385659.1:n.189+55_189+59del
ENST00000449323.5:c.189+55_189+59del	ENSP00000408482.1:n.189+55_189+59del
ENST00000468810.1:n.202_206del
ENST00000478196.6:n.226+55_226+59del
ENST00000495843.1:n.274_278del
NM_001135592.2:c.189+55_189+59del	NP_001129064.1:n.189+55_189+59del
NM_001177413.1:c.189+55_189+59del	NP_001170884.1:n.189+55_189+59del
NM_002954.5:c.189+55_189+59del	NP_002945.1:n.189+55_189+59del
NM_002954.6:c.189+55_189+59del MANE Select	NP_002945.1:n.189+55_189+59del