Canonical Allele Identifier: CA361763150

Gene: RPS14

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150444296C>T , CM000667.2:g.150444296C>T	GRCh38
NC_000005.9:g.149823859C>T , CM000667.1:g.149823859C>T	GRCh37
NC_000005.8:g.149804052C>T	NCBI36
NG_042287.1:g.10461G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312037.6:c.446G>A	ENSP00000311028.5:p.Arg149His
ENST00000401695.8:c.446G>A	ENSP00000385958.3:p.Arg149His
ENST00000407193.7:c.446G>A MANE Select	ENSP00000385425.1:p.Arg149His
ENST00000642507.1:c.446G>A	ENSP00000496665.1:p.Arg149His
ENST00000312037.5:c.446G>A	ENSP00000311028.5:p.Arg149His
ENST00000401695.7:c.446G>A	ENSP00000385958.3:p.Arg149His
ENST00000407193.5:c.446G>A	ENSP00000385425.1:p.Arg149His
ENST00000518139.5:c.*204G>A	ENSP00000429856.1:n.*204G>A
ENST00000519690.1:n.3061G>A
ENST00000521466.5:c.446G>A	ENSP00000428509.1:p.Arg149His
NM_001025070.1:c.446G>A	NP_001020241.1:p.Arg149His
NM_001025071.1:c.446G>A	NP_001020242.1:p.Arg149His
NM_005617.3:c.446G>A	NP_005608.1:p.Arg149His
NM_005617.4:c.446G>A MANE Select	NP_005608.1:p.Arg149His
NM_001025070.2:c.446G>A	NP_001020241.1:p.Arg149His
NM_001025071.2:c.446G>A	NP_001020242.1:p.Arg149His