Canonical Allele Identifier: CA645534661

Gene: RPS27A

Linked Data

• COSMIC: COSM1158841

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55234131_55234132insGAG , CM000664.2:g.55234131_55234132insGAG	GRCh38
NC_000002.11:g.55461267_55461268insGAG , CM000664.1:g.55461267_55461268insGAG	GRCh37
NC_000002.10:g.55314771_55314772insGAG	NCBI36
NG_017017.1:g.7203_7204insGAG
NG_033063.1:g.3432_3433insCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272317.11:c.116_117insGAG MANE Select	ENSP00000272317.6:p.Asp39delinsGluSer
ENST00000272317.10:c.116_117insGAG	ENSP00000272317.6:p.Asp39delinsGluSer
ENST00000402285.7:c.116_117insGAG	ENSP00000383981.3:p.Asp39delinsGluSer
ENST00000404735.1:c.116_117insGAG	ENSP00000385659.1:p.Asp39delinsGluSer
ENST00000449323.5:c.116_117insGAG	ENSP00000408482.1:p.Asp39delinsGluSer
ENST00000468810.1:n.74_75insGAG
ENST00000478196.6:n.153_154insGAG
ENST00000495843.1:n.146_147insGAG
NM_001135592.2:c.116_117insGAG	NP_001129064.1:p.Asp39delinsGluSer
NM_001177413.1:c.116_117insGAG	NP_001170884.1:p.Asp39delinsGluSer
NM_002954.5:c.116_117insGAG	NP_002945.1:p.Asp39delinsGluSer
NM_002954.6:c.116_117insGAG MANE Select	NP_002945.1:p.Asp39delinsGluSer