Canonical Allele Identifier: CA2336668950

Gene: RPS19

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41869258_41869260delinsGCC , CM000681.2:g.41869258_41869260delinsGCC	GRCh38
NC_000019.9:g.42373328_42373330delinsGCC , CM000681.1:g.42373328_42373330delinsGCC	GRCh37
NC_000019.8:g.47065168_47065170delinsGCC	NCBI36
NG_007080.2:g.14341_14343delinsGCC
NG_007080.3:g.14341_14343delinsGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000598742.6:c.356+44_356+46delinsGCC MANE Select	ENSP00000470972.1:n.356+44_356+46delinsGCC
ENST00000600467.6:c.356+44_356+46delinsGCC	ENSP00000469228.2:n.356+44_356+46delinsGCC
ENST00000221975.6:c.134+44_134+46delinsGCC	ENSP00000221975.2:n.134+44_134+46delinsGCC
ENST00000593863.5:c.356+44_356+46delinsGCC	ENSP00000470004.1:n.356+44_356+46delinsGCC
ENST00000598742.5:c.356+44_356+46delinsGCC	ENSP00000470972.1:n.356+44_356+46delinsGCC
NM_001022.3:c.356+44_356+46delinsGCC	NP_001013.1:n.356+44_356+46delinsGCC
NM_001321483.1:c.356+44_356+46delinsGCC	NP_001308412.1:n.356+44_356+46delinsGCC
NM_001321484.1:c.356+44_356+46delinsGCC	NP_001308413.1:n.356+44_356+46delinsGCC
NM_001321485.1:c.369+44_369+46delinsGCC	NP_001308414.1:n.369+44_369+46delinsGCC
XM_017027113.2:c.356+44_356+46delinsGCC	XP_016882602.1:n.356+44_356+46delinsGCC
NM_001022.4:c.356+44_356+46delinsGCC MANE Select	NP_001013.1:n.356+44_356+46delinsGCC
NM_001321483.2:c.356+44_356+46delinsGCC	NP_001308412.1:n.356+44_356+46delinsGCC
NM_001321484.2:c.356+44_356+46delinsGCC	NP_001308413.1:n.356+44_356+46delinsGCC
NM_001321485.2:c.369+44_369+46delinsGCC	NP_001308414.1:n.369+44_369+46delinsGCC