Canonical Allele Identifier: CA2585348967

Gene: RPS19

Linked Data

• gnomAD v4: 19-41869233-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41869233_41869234insA , CM000681.2:g.41869233_41869234insA	GRCh38
NC_000019.9:g.42373303_42373304insA , CM000681.1:g.42373303_42373304insA	GRCh37
NC_000019.8:g.47065143_47065144insA	NCBI36
NG_007080.2:g.14316_14317insA
NG_007080.3:g.14316_14317insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000598742.6:c.356+19_356+20insA MANE Select	ENSP00000470972.1:n.356+19_356+20insA
ENST00000600467.6:c.356+19_356+20insA	ENSP00000469228.2:n.356+19_356+20insA
ENST00000221975.6:c.134+19_134+20insA	ENSP00000221975.2:n.134+19_134+20insA
ENST00000593863.5:c.356+19_356+20insA	ENSP00000470004.1:n.356+19_356+20insA
ENST00000598742.5:c.356+19_356+20insA	ENSP00000470972.1:n.356+19_356+20insA
NM_001022.3:c.356+19_356+20insA	NP_001013.1:n.356+19_356+20insA
NM_001321483.1:c.356+19_356+20insA	NP_001308412.1:n.356+19_356+20insA
NM_001321484.1:c.356+19_356+20insA	NP_001308413.1:n.356+19_356+20insA
NM_001321485.1:c.369+19_369+20insA	NP_001308414.1:n.369+19_369+20insA
XM_017027113.2:c.356+19_356+20insA	XP_016882602.1:n.356+19_356+20insA
NM_001022.4:c.356+19_356+20insA MANE Select	NP_001013.1:n.356+19_356+20insA
NM_001321483.2:c.356+19_356+20insA	NP_001308412.1:n.356+19_356+20insA
NM_001321484.2:c.356+19_356+20insA	NP_001308413.1:n.356+19_356+20insA
NM_001321485.2:c.369+19_369+20insA	NP_001308414.1:n.369+19_369+20insA