Canonical Allele Identifier: CA2695228814

Gene: RPS19

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41869091_41869108del , CM000681.2:g.41869091_41869108del	GRCh38
NC_000019.9:g.42373161_42373178del , CM000681.1:g.42373161_42373178del	GRCh37
NC_000019.8:g.47065001_47065018del	NCBI36
NG_007080.2:g.14174_14191del
NG_007080.3:g.14174_14191del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000598261.2:c.246_263del	ENSP00000469798.1:p.Asp82_Ser87del
ENST00000598742.6:c.233_250del MANE Select	ENSP00000470972.1:p.Ile78_Gln83del
ENST00000600467.6:c.233_250del	ENSP00000469228.2:p.Ile78_Gln83del
ENST00000221975.6:c.11_28del	ENSP00000221975.2:p.Ile4_Gln9del
ENST00000593863.5:c.233_250del	ENSP00000470004.1:p.Ile78_Gln83del
ENST00000598261.1:c.246_263del	ENSP00000469798.1:p.Asp82_Ser87del
ENST00000598399.1:c.1071_1088del	ENSP00000472660.1:n.1071_1088del
ENST00000598742.5:c.233_250del	ENSP00000470972.1:p.Ile78_Gln83del
NM_001022.3:c.233_250del	NP_001013.1:p.Ile78_Gln83del
NM_001321483.1:c.233_250del	NP_001308412.1:p.Ile78_Gln83del
NM_001321484.1:c.233_250del	NP_001308413.1:p.Ile78_Gln83del
NM_001321485.1:c.246_263del	NP_001308414.1:p.Asp82_Ser87del
XM_017027113.2:c.233_250del	XP_016882602.1:p.Ile78_Gln83del
NM_001022.4:c.233_250del MANE Select	NP_001013.1:p.Ile78_Gln83del
NM_001321483.2:c.233_250del	NP_001308412.1:p.Ile78_Gln83del
NM_001321484.2:c.233_250del	NP_001308413.1:p.Ile78_Gln83del
NM_001321485.2:c.246_263del	NP_001308414.1:p.Asp82_Ser87del