Canonical Allele Identifier: CA352211477

Gene: RPSA

Linked Data

• MyVariant Identifiers: chr3:g.39450138C>G (hg19) ; chr3:g.39408647C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39408647C>G , CM000665.2:g.39408647C>G	GRCh38
NC_000003.11:g.39450138C>G , CM000665.1:g.39450138C>G	GRCh37
NC_000003.10:g.39425142C>G	NCBI36
NG_033234.1:g.6935C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000458478.6:c.175C>G	ENSP00000410848.2:p.Leu59Val
ENST00000478027.3:n.725C>G
ENST00000697728.1:c.175C>G	ENSP00000513422.1:p.Leu59Val
ENST00000697729.1:c.175C>G	ENSP00000513423.1:p.Leu59Val
ENST00000697730.1:c.175C>G	ENSP00000513424.1:p.Leu59Val
ENST00000697731.1:c.175C>G	ENSP00000513425.1:p.Leu59Val
ENST00000697732.1:n.163C>G
ENST00000697753.1:c.175C>G	ENSP00000513432.1:p.Leu59Val
ENST00000697816.1:c.*72C>G	ENSP00000513451.1:n.*72C>G
ENST00000301821.11:c.175C>G MANE Select	ENSP00000346067.4:p.Leu59Val
ENST00000301821.10:c.175C>G	ENSP00000346067.4:p.Leu59Val
ENST00000443003.2:c.175C>G	ENSP00000389351.1:p.Leu59Val
ENST00000444512.2:c.175C>G	ENSP00000396716.2:p.Leu59Val
ENST00000458478.5:c.175C>G	ENSP00000410848.1:p.Leu59Val
ENST00000477325.1:n.257C>G
ENST00000478027.2:n.444C>G
NM_001304288.1:c.175C>G	NP_001291217.1:p.Leu59Val
NM_002295.5:c.175C>G	NP_002286.2:p.Leu59Val
NM_002295.6:c.175C>G MANE Select	NP_002286.2:p.Leu59Val
NM_001304288.2:c.175C>G	NP_001291217.1:p.Leu59Val