Canonical Allele Identifier: CA2191414298

Gene: RPS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82540451A= , CM000677.2:g.82540451A=	GRCh38
NC_000015.9:g.82824859A= , CM000677.1:g.82824859A=	GRCh37
NC_000015.8:g.80611914A=	NCBI36
NG_009890.1:g.4787T=
NG_009890.2:g.5094T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560229.6:n.7T=
ENST00000562833.2:c.1351-319T=	ENSP00000454786.2:n.1351-319T=
ENST00000642270.1:c.1358-319T=	ENSP00000496443.1:n.1358-319T=
ENST00000647841.1:c.-23T= MANE Select	ENSP00000498019.1:n.-23T=
ENST00000330244.10:c.-23T=	ENSP00000346046.5:n.-23T=
ENST00000559273.1:n.6T=
ENST00000560229.5:n.7T=
ENST00000560639.1:n.2T=
ENST00000561157.5:c.-23T=	ENSP00000453910.1:n.-23T=
ENST00000562833.1:c.780-319T=
NM_001021.4:c.-23T=	NP_001012.1:n.-23T=
NR_111943.1:n.7T=
NR_111944.1:n.94T=
NM_001021.6:c.-23T= MANE Select	NP_001012.1:n.-23T=
NR_111944.2:n.114T=
NR_111943.2:n.7T=
NR_111944.3:n.7T=