Canonical Allele Identifier: CA2580097319

Gene: RPS19

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41861141del , CM000681.2:g.41861141del	GRCh38
NC_000019.9:g.42365210del , CM000681.1:g.42365210del	GRCh37
NC_000019.8:g.47057050del	NCBI36
NG_007080.2:g.6223del
NG_007080.3:g.6224del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000598261.2:c.101del	ENSP00000469798.1:p.Val34GlyfsTer?
ENST00000598742.6:c.101del MANE Select	ENSP00000470972.1:p.Val34GlyfsTer?
ENST00000600467.6:c.101del	ENSP00000469228.2:p.Val34GlyfsTer?
ENST00000221975.6:c.-122del	ENSP00000221975.2:n.-122del
ENST00000593863.5:c.101del	ENSP00000470004.1:p.Val34GlyfsTer?
ENST00000598261.1:c.101del	ENSP00000469798.1:p.Val34GlyfsTer?
ENST00000598399.1:c.98del	ENSP00000472660.1:p.Val33GlyfsTer?
ENST00000598466.5:n.136del
ENST00000598742.5:c.101del	ENSP00000470972.1:p.Val34GlyfsTer?
ENST00000600467.5:c.101del	ENSP00000469228.1:p.Val34GlyfsTer?
ENST00000601492.5:c.101del	ENSP00000471621.1:p.Val34GlyfsTer27
NM_001022.3:c.101del	NP_001013.1:p.Val34GlyfsTer?
NM_001321483.1:c.101del	NP_001308412.1:p.Val34GlyfsTer?
NM_001321484.1:c.101del	NP_001308413.1:p.Val34GlyfsTer?
NM_001321485.1:c.101del	NP_001308414.1:p.Val34GlyfsTer?
XM_017027113.2:c.101del	XP_016882602.1:p.Val34GlyfsTer?
NM_001022.4:c.101del MANE Select	NP_001013.1:p.Val34GlyfsTer?
NM_001321483.2:c.101del	NP_001308412.1:p.Val34GlyfsTer?
NM_001321484.2:c.101del	NP_001308413.1:p.Val34GlyfsTer?
NM_001321485.2:c.101del	NP_001308414.1:p.Val34GlyfsTer?