Canonical Allele Identifier: CA1252173836

Gene: RPS27A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55234190T= , CM000664.2:g.55234190T=	GRCh38
NC_000002.11:g.55461326T= , CM000664.1:g.55461326T=	GRCh37
NC_000002.10:g.55314830T=	NCBI36
NG_017017.1:g.7262T=
NG_033063.1:g.3374A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272317.11:c.175T= MANE Select	ENSP00000272317.6:p.Tyr59=
ENST00000272317.10:c.175T=	ENSP00000272317.6:p.Tyr59=
ENST00000402285.7:c.175T=	ENSP00000383981.3:p.Tyr59=
ENST00000404735.1:c.175T=	ENSP00000385659.1:p.Tyr59=
ENST00000449323.5:c.175T=	ENSP00000408482.1:p.Tyr59=
ENST00000468810.1:n.133T=
ENST00000478196.6:n.212T=
ENST00000495843.1:n.205T=
NM_001135592.2:c.175T=	NP_001129064.1:p.Tyr59=
NM_001177413.1:c.175T=	NP_001170884.1:p.Tyr59=
NM_002954.5:c.175T=	NP_002945.1:p.Tyr59=
NM_002954.6:c.175T= MANE Select	NP_002945.1:p.Tyr59=