Canonical Allele Identifier: CA1252173785
Gene: RPS27A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.55234088C= , CM000664.2:g.55234088C= GRCh38
NC_000002.11:g.55461224C= , CM000664.1:g.55461224C= GRCh37
NC_000002.10:g.55314728C= NCBI36
NG_017017.1:g.7160C=
NG_033063.1:g.3476G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272317.11:c.104-31C= MANE Select ENSP00000272317.6:n.104-31C=
ENST00000272317.10:c.104-31C= ENSP00000272317.6:n.104-31C=
ENST00000402285.7:c.104-31C= ENSP00000383981.3:n.104-31C=
ENST00000404735.1:c.104-31C= ENSP00000385659.1:n.104-31C=
ENST00000449323.5:c.104-31C= ENSP00000408482.1:n.104-31C=
ENST00000468810.1:n.62-31C=
ENST00000478196.6:n.141-31C=
ENST00000495843.1:n.134-31C=
NM_001135592.2:c.104-31C= NP_001129064.1:n.104-31C=
NM_001177413.1:c.104-31C= NP_001170884.1:n.104-31C=
NM_002954.5:c.104-31C= NP_002945.1:n.104-31C=
NM_002954.6:c.104-31C= MANE Select NP_002945.1:n.104-31C=