Canonical Allele Identifier: CA920112610

Gene: RPS19

Linked Data

• ClinVar Variation Id: 2973066
• ClinVar RCV Id: RCV003830160
• dbSNP Id: rs782448362

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41869228delinsGG , CM000681.2:g.41869228delinsGG	GRCh38
NG_007080.3:g.14311delinsGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000598742.6:c.356+14delinsGG MANE Select	ENSP00000470972.1:n.356+14delinsGG
ENST00000600467.6:c.356+14delinsGG	ENSP00000469228.2:n.356+14delinsGG
ENST00000221975.6:c.134+14delinsGG	ENSP00000221975.2:n.134+14delinsGG
ENST00000593863.5:c.356+14delinsGG	ENSP00000470004.1:n.356+14delinsGG
ENST00000598742.5:c.356+14delinsGG	ENSP00000470972.1:n.356+14delinsGG
NM_001022.3:c.356+14delinsGG	NP_001013.1:n.356+14delinsGG
NM_001321483.1:c.356+14delinsGG	NP_001308412.1:n.356+14delinsGG
NM_001321484.1:c.356+14delinsGG	NP_001308413.1:n.356+14delinsGG
NM_001321485.1:c.369+14delinsGG	NP_001308414.1:n.369+14delinsGG
XM_017027113.2:c.356+14delinsGG	XP_016882602.1:n.356+14delinsGG
NM_001022.4:c.356+14delinsGG MANE Select	NP_001013.1:n.356+14delinsGG
NM_001321483.2:c.356+14delinsGG	NP_001308412.1:n.356+14delinsGG
NM_001321484.2:c.356+14delinsGG	NP_001308413.1:n.356+14delinsGG
NM_001321485.2:c.369+14delinsGG	NP_001308414.1:n.369+14delinsGG