Canonical Allele Identifier: CA406030502

Gene: RPS19

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41869160G>A , CM000681.2:g.41869160G>A	GRCh38
NC_000019.9:g.42373230G>A , CM000681.1:g.42373230G>A	GRCh37
NC_000019.8:g.47065070G>A	NCBI36
NG_007080.2:g.14243G>A
NG_007080.3:g.14243G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001022.4:c.302G>A MANE Select	NP_001013.1:p.Arg101His
ENST00000598742.6:c.302G>A MANE Select	ENSP00000470972.1:p.Arg101His
NM_001022.3:c.302G>A	NP_001013.1:p.Arg101His
NM_001321483.1:c.302G>A	NP_001308412.1:p.Arg101His
NM_001321483.2:c.302G>A	NP_001308412.1:p.Arg101His
NM_001321484.1:c.302G>A	NP_001308413.1:p.Arg101His
NM_001321484.2:c.302G>A	NP_001308413.1:p.Arg101His
NM_001321485.1:c.315G>A	NP_001308414.1:p.Pro105=
NM_001321485.2:c.315G>A	NP_001308414.1:p.Pro105=
ENST00000221975.6:c.80G>A	ENSP00000221975.2:p.Arg27His
ENST00000593863.5:c.302G>A	ENSP00000470004.1:p.Arg101His
ENST00000598399.1:c.1140G>A	ENSP00000472660.1:n.1140G>A
ENST00000598742.5:c.302G>A	ENSP00000470972.1:p.Arg101His
ENST00000600467.6:c.302G>A	ENSP00000469228.2:p.Arg101His
XM_017027113.2:c.302G>A	XP_016882602.1:p.Arg101His