Canonical Allele Identifier: CA1358946036

Gene: RPSA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39408655A= , CM000665.2:g.39408655A=	GRCh38
NC_000003.11:g.39450146A= , CM000665.1:g.39450146A=	GRCh37
NC_000003.10:g.39425150A=	NCBI36
NG_033234.1:g.6943A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000458478.6:c.183A=	ENSP00000410848.2:p.Ala61=
ENST00000478027.3:n.733A=
ENST00000697728.1:c.183A=	ENSP00000513422.1:p.Ala61=
ENST00000697729.1:c.183A=	ENSP00000513423.1:p.Ala61=
ENST00000697730.1:c.183A=	ENSP00000513424.1:p.Ala61=
ENST00000697731.1:c.183A=	ENSP00000513425.1:p.Ala61=
ENST00000697732.1:n.171A=
ENST00000697753.1:c.183A=	ENSP00000513432.1:p.Ala61=
ENST00000697816.1:c.*80A=	ENSP00000513451.1:n.*80A=
ENST00000301821.11:c.183A= MANE Select	ENSP00000346067.4:p.Ala61=
ENST00000301821.10:c.183A=	ENSP00000346067.4:p.Ala61=
ENST00000443003.2:c.183A=	ENSP00000389351.1:p.Ala61=
ENST00000444512.2:c.183A=	ENSP00000396716.2:p.Ala61=
ENST00000458478.5:c.183A=	ENSP00000410848.1:p.Ala61=
ENST00000477325.1:n.265A=
ENST00000478027.2:n.452A=
NM_001304288.1:c.183A=	NP_001291217.1:p.Ala61=
NM_002295.5:c.183A=	NP_002286.2:p.Ala61=
NM_002295.6:c.183A= MANE Select	NP_002286.2:p.Ala61=
NM_001304288.2:c.183A=	NP_001291217.1:p.Ala61=