Canonical Allele Identifier: CA406030605

Gene: RPS19

Linked Data

• MyVariant Identifiers: chr19:g.42373276C>A (hg19) ; chr19:g.41869206C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41869206C>A , CM000681.2:g.41869206C>A	GRCh38
NC_000019.9:g.42373276C>A , CM000681.1:g.42373276C>A	GRCh37
NC_000019.8:g.47065116C>A	NCBI36
NG_007080.2:g.14289C>A
NG_007080.3:g.14289C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000598742.6:c.348C>A MANE Select	ENSP00000470972.1:p.Asp116Glu
ENST00000600467.6:c.348C>A	ENSP00000469228.2:p.Asp116Glu
ENST00000221975.6:c.126C>A	ENSP00000221975.2:p.Asp42Glu
ENST00000593863.5:c.348C>A	ENSP00000470004.1:p.Asp116Glu
ENST00000598742.5:c.348C>A	ENSP00000470972.1:p.Asp116Glu
NM_001022.3:c.348C>A	NP_001013.1:p.Asp116Glu
NM_001321483.1:c.348C>A	NP_001308412.1:p.Asp116Glu
NM_001321484.1:c.348C>A	NP_001308413.1:p.Asp116Glu
NM_001321485.1:c.361C>A	NP_001308414.1:p.Pro121Thr
XM_017027113.2:c.348C>A	XP_016882602.1:p.Asp116Glu
NM_001022.4:c.348C>A MANE Select	NP_001013.1:p.Asp116Glu
NM_001321483.2:c.348C>A	NP_001308412.1:p.Asp116Glu
NM_001321484.2:c.348C>A	NP_001308413.1:p.Asp116Glu
NM_001321485.2:c.361C>A	NP_001308414.1:p.Pro121Thr