Canonical Allele Identifier: CA996008813
Gene: RPS19 HGNC NCBI

Linked Data

dbSNP Id: rs2074115336

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41868866_41868867insG , CM000681.2:g.41868866_41868867insG GRCh38
NC_000019.9:g.42372936_42372937insG , CM000681.1:g.42372936_42372937insG GRCh37
NC_000019.8:g.47064776_47064777insG NCBI36
NG_007080.2:g.13949_13950insG
NG_007080.3:g.13949_13950insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000598261.2:c.186-165_186-164insG ENSP00000469798.1:n.186-165_186-164insG
ENST00000598742.6:c.173-165_173-164insG MANE Select ENSP00000470972.1:n.173-165_173-164insG
ENST00000600467.6:c.173-165_173-164insG ENSP00000469228.2:n.173-165_173-164insG
ENST00000221975.6:c.-50-165_-50-164insG ENSP00000221975.2:n.-50-165_-50-164insG
ENST00000593863.5:c.173-165_173-164insG ENSP00000470004.1:n.173-165_173-164insG
ENST00000598261.1:c.186-165_186-164insG ENSP00000469798.1:n.186-165_186-164insG
ENST00000598399.1:c.1011-165_1011-164insG ENSP00000472660.1:n.1011-165_1011-164insG
ENST00000598742.5:c.173-165_173-164insG ENSP00000470972.1:n.173-165_173-164insG
ENST00000600467.5:c.173-165_173-164insG ENSP00000469228.1:n.173-165_173-164insG
ENST00000601492.5:c.254-165_254-164insG ENSP00000471621.1:n.254-165_254-164insG
NM_001022.3:c.173-165_173-164insG NP_001013.1:n.173-165_173-164insG
NM_001321483.1:c.173-165_173-164insG NP_001308412.1:n.173-165_173-164insG
NM_001321484.1:c.173-165_173-164insG NP_001308413.1:n.173-165_173-164insG
NM_001321485.1:c.186-165_186-164insG NP_001308414.1:n.186-165_186-164insG
XM_017027113.2:c.173-165_173-164insG XP_016882602.1:n.173-165_173-164insG
NM_001022.4:c.173-165_173-164insG MANE Select NP_001013.1:n.173-165_173-164insG
NM_001321483.2:c.173-165_173-164insG NP_001308412.1:n.173-165_173-164insG
NM_001321484.2:c.173-165_173-164insG NP_001308413.1:n.173-165_173-164insG
NM_001321485.2:c.186-165_186-164insG NP_001308414.1:n.186-165_186-164insG