Canonical Allele Identifier: CA2191414126

Gene: RPS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82540337C= , CM000677.2:g.82540337C=	GRCh38
NC_000015.9:g.82824745C= , CM000677.1:g.82824745C=	GRCh37
NC_000015.8:g.80611800C=	NCBI36
NG_009890.1:g.4901G=
NG_009890.2:g.5208G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000560229.6:n.121G=
ENST00000562833.2:c.1351-205G=	ENSP00000454786.2:n.1351-205G=
ENST00000642270.1:c.1358-205G=	ENSP00000496443.1:n.1358-205G=
ENST00000647841.1:c.3+89G= MANE Select	ENSP00000498019.1:n.3+89G=
ENST00000330244.10:c.3+89G=	ENSP00000346046.5:n.3+89G=
ENST00000558397.1:c.3+89G=	ENSP00000452889.1:n.3+89G=
ENST00000559273.1:n.31+89G=
ENST00000559776.1:n.83G=
ENST00000560229.5:n.121G=
ENST00000560639.1:n.27+89G=
ENST00000561157.5:c.3+89G=	ENSP00000453910.1:n.3+89G=
ENST00000562833.1:c.780-205G=
NM_001021.4:c.3+89G=	NP_001012.1:n.3+89G=
NR_111943.1:n.121G=
NR_111944.1:n.119+89G=
NM_001021.6:c.3+89G= MANE Select	NP_001012.1:n.3+89G=
NR_111944.2:n.139+89G=
NR_111943.2:n.121G=
NR_111944.3:n.32+89G=