Canonical Allele Identifier: CA2336668878
Gene: RPS19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41869108A= , CM000681.2:g.41869108A= GRCh38
NC_000019.9:g.42373178A= , CM000681.1:g.42373178A= GRCh37
NC_000019.8:g.47065018A= NCBI36
NG_007080.2:g.14191A=
NG_007080.3:g.14191A=

Transcript Alleles

HGVS Amino-acid change
ENST00000598261.2:c.263A= ENSP00000469798.1:p.Glu88=
ENST00000598742.6:c.250A= MANE Select ENSP00000470972.1:p.Arg84=
ENST00000600467.6:c.250A= ENSP00000469228.2:p.Arg84=
ENST00000221975.6:c.28A= ENSP00000221975.2:p.Arg10=
ENST00000593863.5:c.250A= ENSP00000470004.1:p.Arg84=
ENST00000598261.1:c.263A= ENSP00000469798.1:p.Glu88=
ENST00000598399.1:c.1088A= ENSP00000472660.1:n.1088A=
ENST00000598742.5:c.250A= ENSP00000470972.1:p.Arg84=
NM_001022.3:c.250A= NP_001013.1:p.Arg84=
NM_001321483.1:c.250A= NP_001308412.1:p.Arg84=
NM_001321484.1:c.250A= NP_001308413.1:p.Arg84=
NM_001321485.1:c.263A= NP_001308414.1:p.Glu88=
XM_017027113.2:c.250A= XP_016882602.1:p.Arg84=
NM_001022.4:c.250A= MANE Select NP_001013.1:p.Arg84=
NM_001321483.2:c.250A= NP_001308412.1:p.Arg84=
NM_001321484.2:c.250A= NP_001308413.1:p.Arg84=
NM_001321485.2:c.263A= NP_001308414.1:p.Glu88=