Canonical Allele Identifier: CA346904079

Gene: RPS27A

Linked Data

• MyVariant Identifiers: chr2:g.55461328C>G (hg19) ; chr2:g.55234192C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55234192C>G , CM000664.2:g.55234192C>G	GRCh38
NC_000002.11:g.55461328C>G , CM000664.1:g.55461328C>G	GRCh37
NC_000002.10:g.55314832C>G	NCBI36
NG_017017.1:g.7264C>G
NG_033063.1:g.3372G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272317.11:c.177C>G MANE Select	ENSP00000272317.6:p.Tyr59Ter
ENST00000272317.10:c.177C>G	ENSP00000272317.6:p.Tyr59Ter
ENST00000402285.7:c.177C>G	ENSP00000383981.3:p.Tyr59Ter
ENST00000404735.1:c.177C>G	ENSP00000385659.1:p.Tyr59Ter
ENST00000449323.5:c.177C>G	ENSP00000408482.1:p.Tyr59Ter
ENST00000468810.1:n.135C>G
ENST00000478196.6:n.214C>G
ENST00000495843.1:n.207C>G
NM_001135592.2:c.177C>G	NP_001129064.1:p.Tyr59Ter
NM_001177413.1:c.177C>G	NP_001170884.1:p.Tyr59Ter
NM_002954.5:c.177C>G	NP_002945.1:p.Tyr59Ter
NM_002954.6:c.177C>G MANE Select	NP_002945.1:p.Tyr59Ter