Canonical Allele Identifier: CA2191414250

Gene: RPS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82540427A= , CM000677.2:g.82540427A=	GRCh38
NC_000015.9:g.82824835A= , CM000677.1:g.82824835A=	GRCh37
NC_000015.8:g.80611890A=	NCBI36
NG_009890.1:g.4811T=
NG_009890.2:g.5118T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001021.6:c.2T= MANE Select	NP_001012.1:p.Met1=
ENST00000647841.1:c.2T= MANE Select	ENSP00000498019.1:p.Met1=
NM_001021.4:c.2T=	NP_001012.1:p.Met1=
NR_111943.1:n.31T=
NR_111943.2:n.31T=
NR_111944.1:n.118T=
NR_111944.2:n.138T=
NR_111944.3:n.31T=
ENST00000330244.10:c.2T=	ENSP00000346046.5:p.Met1=
ENST00000558397.1:c.2T=	ENSP00000452889.1:p.Met1=
ENST00000559273.1:n.30T=
ENST00000560229.5:n.31T=
ENST00000560229.6:n.31T=
ENST00000560639.1:n.26T=
ENST00000561157.5:c.2T=	ENSP00000453910.1:p.Met1=
ENST00000562833.1:c.780-295T=
ENST00000562833.2:c.1351-295T=	ENSP00000454786.2:n.1351-295T=
ENST00000642270.1:c.1358-295T=	ENSP00000496443.1:n.1358-295T=