Canonical Allele Identifier: CA2336668933

Gene: RPS19

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41869227_41869228delinsGA , CM000681.2:g.41869227_41869228delinsGA	GRCh38
NG_007080.3:g.14310_14311delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000598742.6:c.356+13_356+14delinsGA MANE Select	ENSP00000470972.1:n.356+13_356+14delinsGA
ENST00000600467.6:c.356+13_356+14delinsGA	ENSP00000469228.2:n.356+13_356+14delinsGA
ENST00000221975.6:c.134+13_134+14delinsGA	ENSP00000221975.2:n.134+13_134+14delinsGA
ENST00000593863.5:c.356+13_356+14delinsGA	ENSP00000470004.1:n.356+13_356+14delinsGA
ENST00000598742.5:c.356+13_356+14delinsGA	ENSP00000470972.1:n.356+13_356+14delinsGA
NM_001022.3:c.356+13_356+14delinsGA	NP_001013.1:n.356+13_356+14delinsGA
NM_001321483.1:c.356+13_356+14delinsGA	NP_001308412.1:n.356+13_356+14delinsGA
NM_001321484.1:c.356+13_356+14delinsGA	NP_001308413.1:n.356+13_356+14delinsGA
NM_001321485.1:c.369+13_369+14delinsGA	NP_001308414.1:n.369+13_369+14delinsGA
XM_017027113.2:c.356+13_356+14delinsGA	XP_016882602.1:n.356+13_356+14delinsGA
NM_001022.4:c.356+13_356+14delinsGA MANE Select	NP_001013.1:n.356+13_356+14delinsGA
NM_001321483.2:c.356+13_356+14delinsGA	NP_001308412.1:n.356+13_356+14delinsGA
NM_001321484.2:c.356+13_356+14delinsGA	NP_001308413.1:n.356+13_356+14delinsGA
NM_001321485.2:c.369+13_369+14delinsGA	NP_001308414.1:n.369+13_369+14delinsGA