Canonical Allele Identifier: CA2529609816

Gene: RPS19

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41868862_41868863del , CM000681.2:g.41868862_41868863del	GRCh38
NC_000019.9:g.42372932_42372933del , CM000681.1:g.42372932_42372933del	GRCh37
NC_000019.8:g.47064772_47064773del	NCBI36
NG_007080.2:g.13945_13946del
NG_007080.3:g.13945_13946del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000598261.2:c.186-169_186-168del	ENSP00000469798.1:n.186-169_186-168del
ENST00000598742.6:c.173-169_173-168del MANE Select	ENSP00000470972.1:n.173-169_173-168del
ENST00000600467.6:c.173-169_173-168del	ENSP00000469228.2:n.173-169_173-168del
ENST00000221975.6:c.-50-169_-50-168del	ENSP00000221975.2:n.-50-169_-50-168del
ENST00000593863.5:c.173-169_173-168del	ENSP00000470004.1:n.173-169_173-168del
ENST00000598261.1:c.186-169_186-168del	ENSP00000469798.1:n.186-169_186-168del
ENST00000598399.1:c.1011-169_1011-168del	ENSP00000472660.1:n.1011-169_1011-168del
ENST00000598742.5:c.173-169_173-168del	ENSP00000470972.1:n.173-169_173-168del
ENST00000600467.5:c.173-169_173-168del	ENSP00000469228.1:n.173-169_173-168del
ENST00000601492.5:c.254-169_254-168del	ENSP00000471621.1:n.254-169_254-168del
NM_001022.3:c.173-169_173-168del	NP_001013.1:n.173-169_173-168del
NM_001321483.1:c.173-169_173-168del	NP_001308412.1:n.173-169_173-168del
NM_001321484.1:c.173-169_173-168del	NP_001308413.1:n.173-169_173-168del
NM_001321485.1:c.186-169_186-168del	NP_001308414.1:n.186-169_186-168del
XM_017027113.2:c.173-169_173-168del	XP_016882602.1:n.173-169_173-168del
NM_001022.4:c.173-169_173-168del MANE Select	NP_001013.1:n.173-169_173-168del
NM_001321483.2:c.173-169_173-168del	NP_001308412.1:n.173-169_173-168del
NM_001321484.2:c.173-169_173-168del	NP_001308413.1:n.173-169_173-168del
NM_001321485.2:c.186-169_186-168del	NP_001308414.1:n.186-169_186-168del