Canonical Allele Identifier: CA906969314

Gene: RPSA

Linked Data

• dbSNP Id: rs1284449855
• MyVariant Identifiers: chr3:g.39450059C>T (hg19) ; chr3:g.39408568C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39408568C>T , CM000665.2:g.39408568C>T	GRCh38
NC_000003.11:g.39450059C>T , CM000665.1:g.39450059C>T	GRCh37
NC_000003.10:g.39425063C>T	NCBI36
NG_033234.1:g.6856C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000458478.6:c.134-38C>T	ENSP00000410848.2:n.134-38C>T
ENST00000478027.3:n.646C>T
ENST00000697728.1:c.134-38C>T	ENSP00000513422.1:n.134-38C>T
ENST00000697729.1:c.134-38C>T	ENSP00000513423.1:n.134-38C>T
ENST00000697730.1:c.134-38C>T	ENSP00000513424.1:n.134-38C>T
ENST00000697731.1:c.134-38C>T	ENSP00000513425.1:n.134-38C>T
ENST00000697732.1:n.122-38C>T
ENST00000697753.1:c.134-38C>T	ENSP00000513432.1:n.134-38C>T
ENST00000697816.1:c.*31-38C>T	ENSP00000513451.1:n.*31-38C>T
ENST00000301821.11:c.134-38C>T MANE Select	ENSP00000346067.4:n.134-38C>T
ENST00000301821.10:c.134-38C>T	ENSP00000346067.4:n.134-38C>T
ENST00000443003.2:c.134-38C>T	ENSP00000389351.1:n.134-38C>T
ENST00000444512.2:c.134-38C>T	ENSP00000396716.2:n.134-38C>T
ENST00000458478.5:c.134-38C>T	ENSP00000410848.1:n.134-38C>T
ENST00000477325.1:n.216-38C>T
ENST00000478027.2:n.365C>T
NM_001304288.1:c.134-38C>T	NP_001291217.1:n.134-38C>T
NM_002295.5:c.134-38C>T	NP_002286.2:n.134-38C>T
NM_002295.6:c.134-38C>T MANE Select	NP_002286.2:n.134-38C>T
NM_001304288.2:c.134-38C>T	NP_001291217.1:n.134-38C>T