Canonical Allele Identifier: CA1252173888

Gene: RPS27A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55234270_55234275delinsCTTTTT , CM000664.2:g.55234270_55234275delinsCTTTTT	GRCh38
NC_000002.11:g.55461406_55461411delinsCTTTTT , CM000664.1:g.55461406_55461411delinsCTTTTT	GRCh37
NC_000002.10:g.55314910_55314915delinsCTTTTT	NCBI36
NG_017017.1:g.7342_7347delinsCTTTTT
NG_033063.1:g.3289_3294delinsAAAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272317.11:c.189+66_189+71delinsCTTTTT MANE Select	ENSP00000272317.6:n.189+66_189+71delinsCTTTTT
ENST00000272317.10:c.189+66_189+71delinsCTTTTT	ENSP00000272317.6:n.189+66_189+71delinsCTTTTT
ENST00000402285.7:c.189+66_189+71delinsCTTTTT	ENSP00000383981.3:n.189+66_189+71delinsCTTTTT
ENST00000404735.1:c.189+66_189+71delinsCTTTTT	ENSP00000385659.1:n.189+66_189+71delinsCTTTTT
ENST00000449323.5:c.189+66_189+71delinsCTTTTT	ENSP00000408482.1:n.189+66_189+71delinsCTTTTT
ENST00000468810.1:n.213_218delinsCTTTTT
ENST00000478196.6:n.226+66_226+71delinsCTTTTT
ENST00000495843.1:n.285_290delinsCTTTTT
NM_001135592.2:c.189+66_189+71delinsCTTTTT	NP_001129064.1:n.189+66_189+71delinsCTTTTT
NM_001177413.1:c.189+66_189+71delinsCTTTTT	NP_001170884.1:n.189+66_189+71delinsCTTTTT
NM_002954.5:c.189+66_189+71delinsCTTTTT	NP_002945.1:n.189+66_189+71delinsCTTTTT
NM_002954.6:c.189+66_189+71delinsCTTTTT MANE Select	NP_002945.1:n.189+66_189+71delinsCTTTTT