Canonical Allele Identifier: CA2573156359

Gene: RPS19

Linked Data

• ClinVar Variation Id: 1586153
• ClinVar RCV Id: RCV002104757
• dbSNP Id: rs2123283596

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41869023_41869024delinsTT , CM000681.2:g.41869023_41869024delinsTT	GRCh38
NC_000019.9:g.42373093_42373094delinsTT , CM000681.1:g.42373093_42373094delinsTT	GRCh37
NC_000019.8:g.47064933_47064934delinsTT	NCBI36
NG_007080.2:g.14106_14107delinsTT
NG_007080.3:g.14106_14107delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000598261.2:c.186-8_186-7delinsTT	ENSP00000469798.1:n.186-8_186-7delinsTT
ENST00000598742.6:c.173-8_173-7delinsTT MANE Select	ENSP00000470972.1:n.173-8_173-7delinsTT
ENST00000600467.6:c.173-8_173-7delinsTT	ENSP00000469228.2:n.173-8_173-7delinsTT
ENST00000221975.6:c.-50-8_-50-7delinsTT	ENSP00000221975.2:n.-50-8_-50-7delinsTT
ENST00000593863.5:c.173-8_173-7delinsTT	ENSP00000470004.1:n.173-8_173-7delinsTT
ENST00000598261.1:c.186-8_186-7delinsTT	ENSP00000469798.1:n.186-8_186-7delinsTT
ENST00000598399.1:c.1011-8_1011-7delinsTT	ENSP00000472660.1:n.1011-8_1011-7delinsTT
ENST00000598742.5:c.173-8_173-7delinsTT	ENSP00000470972.1:n.173-8_173-7delinsTT
ENST00000600467.5:c.173-8_173-7delinsTT	ENSP00000469228.1:n.173-8_173-7delinsTT
ENST00000601492.5:c.254-8_254-7delinsTT	ENSP00000471621.1:n.254-8_254-7delinsTT
NM_001022.3:c.173-8_173-7delinsTT	NP_001013.1:n.173-8_173-7delinsTT
NM_001321483.1:c.173-8_173-7delinsTT	NP_001308412.1:n.173-8_173-7delinsTT
NM_001321484.1:c.173-8_173-7delinsTT	NP_001308413.1:n.173-8_173-7delinsTT
NM_001321485.1:c.186-8_186-7delinsTT	NP_001308414.1:n.186-8_186-7delinsTT
XM_017027113.2:c.173-8_173-7delinsTT	XP_016882602.1:n.173-8_173-7delinsTT
NM_001022.4:c.173-8_173-7delinsTT MANE Select	NP_001013.1:n.173-8_173-7delinsTT
NM_001321483.2:c.173-8_173-7delinsTT	NP_001308412.1:n.173-8_173-7delinsTT
NM_001321484.2:c.173-8_173-7delinsTT	NP_001308413.1:n.173-8_173-7delinsTT
NM_001321485.2:c.186-8_186-7delinsTT	NP_001308414.1:n.186-8_186-7delinsTT