Canonical Allele Identifier: CA352211486

Gene: RPSA

Linked Data

• MyVariant Identifiers: chr3:g.39450141C>A (hg19) ; chr3:g.39408650C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39408650C>A , CM000665.2:g.39408650C>A	GRCh38
NC_000003.11:g.39450141C>A , CM000665.1:g.39450141C>A	GRCh37
NC_000003.10:g.39425145C>A	NCBI36
NG_033234.1:g.6938C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000458478.6:c.178C>A	ENSP00000410848.2:p.Leu60Met
ENST00000478027.3:n.728C>A
ENST00000697728.1:c.178C>A	ENSP00000513422.1:p.Leu60Met
ENST00000697729.1:c.178C>A	ENSP00000513423.1:p.Leu60Met
ENST00000697730.1:c.178C>A	ENSP00000513424.1:p.Leu60Met
ENST00000697731.1:c.178C>A	ENSP00000513425.1:p.Leu60Met
ENST00000697732.1:n.166C>A
ENST00000697753.1:c.178C>A	ENSP00000513432.1:p.Leu60Met
ENST00000697816.1:c.*75C>A	ENSP00000513451.1:n.*75C>A
ENST00000301821.11:c.178C>A MANE Select	ENSP00000346067.4:p.Leu60Met
ENST00000301821.10:c.178C>A	ENSP00000346067.4:p.Leu60Met
ENST00000443003.2:c.178C>A	ENSP00000389351.1:p.Leu60Met
ENST00000444512.2:c.178C>A	ENSP00000396716.2:p.Leu60Met
ENST00000458478.5:c.178C>A	ENSP00000410848.1:p.Leu60Met
ENST00000477325.1:n.260C>A
ENST00000478027.2:n.447C>A
NM_001304288.1:c.178C>A	NP_001291217.1:p.Leu60Met
NM_002295.5:c.178C>A	NP_002286.2:p.Leu60Met
NM_002295.6:c.178C>A MANE Select	NP_002286.2:p.Leu60Met
NM_001304288.2:c.178C>A	NP_001291217.1:p.Leu60Met