Canonical Allele Identifier: CA352211478

Gene: RPSA

Linked Data

• MyVariant Identifiers: chr3:g.39450139T>C (hg19) ; chr3:g.39408648T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39408648T>C , CM000665.2:g.39408648T>C	GRCh38
NC_000003.11:g.39450139T>C , CM000665.1:g.39450139T>C	GRCh37
NC_000003.10:g.39425143T>C	NCBI36
NG_033234.1:g.6936T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000458478.6:c.176T>C	ENSP00000410848.2:p.Leu59Pro
ENST00000478027.3:n.726T>C
ENST00000697728.1:c.176T>C	ENSP00000513422.1:p.Leu59Pro
ENST00000697729.1:c.176T>C	ENSP00000513423.1:p.Leu59Pro
ENST00000697730.1:c.176T>C	ENSP00000513424.1:p.Leu59Pro
ENST00000697731.1:c.176T>C	ENSP00000513425.1:p.Leu59Pro
ENST00000697732.1:n.164T>C
ENST00000697753.1:c.176T>C	ENSP00000513432.1:p.Leu59Pro
ENST00000697816.1:c.*73T>C	ENSP00000513451.1:n.*73T>C
ENST00000301821.11:c.176T>C MANE Select	ENSP00000346067.4:p.Leu59Pro
ENST00000301821.10:c.176T>C	ENSP00000346067.4:p.Leu59Pro
ENST00000443003.2:c.176T>C	ENSP00000389351.1:p.Leu59Pro
ENST00000444512.2:c.176T>C	ENSP00000396716.2:p.Leu59Pro
ENST00000458478.5:c.176T>C	ENSP00000410848.1:p.Leu59Pro
ENST00000477325.1:n.258T>C
ENST00000478027.2:n.445T>C
NM_001304288.1:c.176T>C	NP_001291217.1:p.Leu59Pro
NM_002295.5:c.176T>C	NP_002286.2:p.Leu59Pro
NM_002295.6:c.176T>C MANE Select	NP_002286.2:p.Leu59Pro
NM_001304288.2:c.176T>C	NP_001291217.1:p.Leu59Pro