Canonical Allele Identifier: CA1252173897
Gene: RPS27A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.55234291_55234293delinsACT , CM000664.2:g.55234291_55234293delinsACT GRCh38
NC_000002.11:g.55461427_55461429delinsACT , CM000664.1:g.55461427_55461429delinsACT GRCh37
NC_000002.10:g.55314931_55314933delinsACT NCBI36
NG_017017.1:g.7363_7365delinsACT
NG_033063.1:g.3271_3273delinsAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000272317.11:c.189+87_189+89delinsACT MANE Select ENSP00000272317.6:n.189+87_189+89delinsACT
ENST00000272317.10:c.189+87_189+89delinsACT ENSP00000272317.6:n.189+87_189+89delinsACT
ENST00000402285.7:c.189+87_189+89delinsACT ENSP00000383981.3:n.189+87_189+89delinsACT
ENST00000404735.1:c.189+87_189+89delinsACT ENSP00000385659.1:n.189+87_189+89delinsACT
ENST00000449323.5:c.189+87_189+89delinsACT ENSP00000408482.1:n.189+87_189+89delinsACT
ENST00000468810.1:n.234_236delinsACT
ENST00000478196.6:n.226+87_226+89delinsACT
ENST00000495843.1:n.306_308delinsACT
NM_001135592.2:c.189+87_189+89delinsACT NP_001129064.1:n.189+87_189+89delinsACT
NM_001177413.1:c.189+87_189+89delinsACT NP_001170884.1:n.189+87_189+89delinsACT
NM_002954.5:c.189+87_189+89delinsACT NP_002945.1:n.189+87_189+89delinsACT
NM_002954.6:c.189+87_189+89delinsACT MANE Select NP_002945.1:n.189+87_189+89delinsACT