Canonical Allele Identifier: CA2336668916

Gene: RPS19

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41869191A= , CM000681.2:g.41869191A=	GRCh38
NC_000019.9:g.42373261A= , CM000681.1:g.42373261A=	GRCh37
NC_000019.8:g.47065101A=	NCBI36
NG_007080.2:g.14274A=
NG_007080.3:g.14274A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000598742.6:c.333A= MANE Select	ENSP00000470972.1:p.Lys111=
ENST00000600467.6:c.333A=	ENSP00000469228.2:p.Lys111=
ENST00000221975.6:c.111A=	ENSP00000221975.2:p.Lys37=
ENST00000593863.5:c.333A=	ENSP00000470004.1:p.Lys111=
ENST00000598399.1:c.1171A=	ENSP00000472660.1:n.1171A=
ENST00000598742.5:c.333A=	ENSP00000470972.1:p.Lys111=
NM_001022.3:c.333A=	NP_001013.1:p.Lys111=
NM_001321483.1:c.333A=	NP_001308412.1:p.Lys111=
NM_001321484.1:c.333A=	NP_001308413.1:p.Lys111=
NM_001321485.1:c.346A=	NP_001308414.1:p.Asn116=
XM_017027113.2:c.333A=	XP_016882602.1:p.Lys111=
NM_001022.4:c.333A= MANE Select	NP_001013.1:p.Lys111=
NM_001321483.2:c.333A=	NP_001308412.1:p.Lys111=
NM_001321484.2:c.333A=	NP_001308413.1:p.Lys111=
NM_001321485.2:c.346A=	NP_001308414.1:p.Asn116=