Canonical Allele Identifier: CA2336664149

Gene: RPS19

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41860817G= , CM000681.2:g.41860817G=	GRCh38
NC_000019.9:g.42364887G= , CM000681.1:g.42364887G=	GRCh37
NC_000019.8:g.47056727G=	NCBI36
NG_007080.2:g.5900G=
NG_007080.3:g.5900G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001022.4:c.43G= MANE Select	NP_001013.1:p.Val15=
ENST00000598742.6:c.43G= MANE Select	ENSP00000470972.1:p.Val15=
NM_001022.3:c.43G=	NP_001013.1:p.Val15=
NM_001321483.1:c.43G=	NP_001308412.1:p.Val15=
NM_001321483.2:c.43G=	NP_001308412.1:p.Val15=
NM_001321484.1:c.43G=	NP_001308413.1:p.Val15=
NM_001321484.2:c.43G=	NP_001308413.1:p.Val15=
NM_001321485.1:c.43G=	NP_001308414.1:p.Val15=
NM_001321485.2:c.43G=	NP_001308414.1:p.Val15=
ENST00000221975.6:c.-180G=	ENSP00000221975.2:n.-180G=
ENST00000593863.5:c.43G=	ENSP00000470004.1:p.Val15=
ENST00000598261.1:c.43G=	ENSP00000469798.1:p.Val15=
ENST00000598261.2:c.43G=	ENSP00000469798.1:p.Val15=
ENST00000598399.1:c.40G=	ENSP00000472660.1:p.Val14=
ENST00000598466.5:n.78G=
ENST00000598742.5:c.43G=	ENSP00000470972.1:p.Val15=
ENST00000600467.5:c.43G=	ENSP00000469228.1:p.Val15=
ENST00000600467.6:c.43G=	ENSP00000469228.2:p.Val15=
ENST00000601492.5:c.43G=	ENSP00000471621.1:p.Val15=
XM_017027113.2:c.43G=	XP_016882602.1:p.Val15=