Canonical Allele Identifier: CA2336668883

Gene: RPS19

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41869116C= , CM000681.2:g.41869116C=	GRCh38
NC_000019.9:g.42373186C= , CM000681.1:g.42373186C=	GRCh37
NC_000019.8:g.47065026C=	NCBI36
NG_007080.2:g.14199C=
NG_007080.3:g.14199C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000598261.2:c.271C=	ENSP00000469798.1:p.Arg91=
ENST00000598742.6:c.258C= MANE Select	ENSP00000470972.1:p.Gly86=
ENST00000600467.6:c.258C=	ENSP00000469228.2:p.Gly86=
ENST00000221975.6:c.36C=	ENSP00000221975.2:p.Gly12=
ENST00000593863.5:c.258C=	ENSP00000470004.1:p.Gly86=
ENST00000598261.1:c.271C=	ENSP00000469798.1:p.Arg91=
ENST00000598399.1:c.1096C=	ENSP00000472660.1:n.1096C=
ENST00000598742.5:c.258C=	ENSP00000470972.1:p.Gly86=
NM_001022.3:c.258C=	NP_001013.1:p.Gly86=
NM_001321483.1:c.258C=	NP_001308412.1:p.Gly86=
NM_001321484.1:c.258C=	NP_001308413.1:p.Gly86=
NM_001321485.1:c.271C=	NP_001308414.1:p.Arg91=
XM_017027113.2:c.258C=	XP_016882602.1:p.Gly86=
NM_001022.4:c.258C= MANE Select	NP_001013.1:p.Gly86=
NM_001321483.2:c.258C=	NP_001308412.1:p.Gly86=
NM_001321484.2:c.258C=	NP_001308413.1:p.Gly86=
NM_001321485.2:c.271C=	NP_001308414.1:p.Arg91=