Canonical Allele Identifier: CA882375300

Gene: RPS19

Linked Data

• dbSNP Id: rs782609455
• gnomAD v3: 19-41869227-GA-G
• gnomAD v4: 19-41869227-GA-G
• MyVariant Identifiers: chr19:g.41869228del (hg38)

Genomic Alleles

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

Transcript Alleles

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