Canonical Allele Identifier: CA1358945997

Gene: RPSA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39408565C= , CM000665.2:g.39408565C=	GRCh38
NC_000003.11:g.39450056C= , CM000665.1:g.39450056C=	GRCh37
NC_000003.10:g.39425060C=	NCBI36
NG_033234.1:g.6853C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000458478.6:c.134-41C=	ENSP00000410848.2:n.134-41C=
ENST00000478027.3:n.643C=
ENST00000697728.1:c.134-41C=	ENSP00000513422.1:n.134-41C=
ENST00000697729.1:c.134-41C=	ENSP00000513423.1:n.134-41C=
ENST00000697730.1:c.134-41C=	ENSP00000513424.1:n.134-41C=
ENST00000697731.1:c.134-41C=	ENSP00000513425.1:n.134-41C=
ENST00000697732.1:n.122-41C=
ENST00000697753.1:c.134-41C=	ENSP00000513432.1:n.134-41C=
ENST00000697816.1:c.*31-41C=	ENSP00000513451.1:n.*31-41C=
ENST00000301821.11:c.134-41C= MANE Select	ENSP00000346067.4:n.134-41C=
ENST00000301821.10:c.134-41C=	ENSP00000346067.4:n.134-41C=
ENST00000443003.2:c.134-41C=	ENSP00000389351.1:n.134-41C=
ENST00000444512.2:c.134-41C=	ENSP00000396716.2:n.134-41C=
ENST00000458478.5:c.134-41C=	ENSP00000410848.1:n.134-41C=
ENST00000477325.1:n.216-41C=
ENST00000478027.2:n.362C=
NM_001304288.1:c.134-41C=	NP_001291217.1:n.134-41C=
NM_002295.5:c.134-41C=	NP_002286.2:n.134-41C=
NM_002295.6:c.134-41C= MANE Select	NP_002286.2:n.134-41C=
NM_001304288.2:c.134-41C=	NP_001291217.1:n.134-41C=