Canonical Allele Identifier: CA2695228817

Gene: RPS19

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41869101dup , CM000681.2:g.41869101dup	GRCh38
NC_000019.9:g.42373171dup , CM000681.1:g.42373171dup	GRCh37
NC_000019.8:g.47065011dup	NCBI36
NG_007080.2:g.14184dup
NG_007080.3:g.14184dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000598261.2:c.256dup	ENSP00000469798.1:p.Thr86AsnfsTer?
ENST00000598742.6:c.243dup MANE Select	ENSP00000470972.1:p.Arg82ThrfsTer?
ENST00000600467.6:c.243dup	ENSP00000469228.2:p.Arg82ThrfsTer?
ENST00000221975.6:c.21dup	ENSP00000221975.2:p.Arg8ThrfsTer?
ENST00000593863.5:c.243dup	ENSP00000470004.1:p.Arg82ThrfsTer?
ENST00000598261.1:c.256dup	ENSP00000469798.1:p.Thr86AsnfsTer?
ENST00000598399.1:c.1081dup	ENSP00000472660.1:n.1081dup
ENST00000598742.5:c.243dup	ENSP00000470972.1:p.Arg82ThrfsTer?
NM_001022.3:c.243dup	NP_001013.1:p.Arg82ThrfsTer?
NM_001321483.1:c.243dup	NP_001308412.1:p.Arg82ThrfsTer?
NM_001321484.1:c.243dup	NP_001308413.1:p.Arg82ThrfsTer?
NM_001321485.1:c.256dup	NP_001308414.1:p.Thr86AsnfsTer30
XM_017027113.2:c.243dup	XP_016882602.1:p.Arg82ThrfsTer?
NM_001022.4:c.243dup MANE Select	NP_001013.1:p.Arg82ThrfsTer?
NM_001321483.2:c.243dup	NP_001308412.1:p.Arg82ThrfsTer?
NM_001321484.2:c.243dup	NP_001308413.1:p.Arg82ThrfsTer?
NM_001321485.2:c.256dup	NP_001308414.1:p.Thr86AsnfsTer30