Canonical Allele Identifier: CA2191414120

Gene: RPS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82540329_82540330delinsCT , CM000677.2:g.82540329_82540330delinsCT	GRCh38
NC_000015.9:g.82824737_82824738delinsCT , CM000677.1:g.82824737_82824738delinsCT	GRCh37
NC_000015.8:g.80611792_80611793delinsCT	NCBI36
NG_009890.1:g.4908_4909delinsAG
NG_009890.2:g.5215_5216delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000560229.6:n.128_129delinsAG
ENST00000562833.2:c.1351-198_1351-197delinsAG	ENSP00000454786.2:n.1351-198_1351-197deli...
ENST00000642270.1:c.1358-198_1358-197delinsAG	ENSP00000496443.1:n.1358-198_1358-197deli...
ENST00000647841.1:c.3+96_3+97delinsAG MANE Select	ENSP00000498019.1:n.3+96_3+97delinsAG
ENST00000330244.10:c.3+96_3+97delinsAG	ENSP00000346046.5:n.3+96_3+97delinsAG
ENST00000558397.1:c.3+96_3+97delinsAG	ENSP00000452889.1:n.3+96_3+97delinsAG
ENST00000559273.1:n.31+96_31+97delinsAG
ENST00000559776.1:n.90_91delinsAG
ENST00000560229.5:n.128_129delinsAG
ENST00000560639.1:n.27+96_27+97delinsAG
ENST00000561157.5:c.3+96_3+97delinsAG	ENSP00000453910.1:n.3+96_3+97delinsAG
ENST00000562833.1:c.780-198_780-197delinsAG
NM_001021.4:c.3+96_3+97delinsAG	NP_001012.1:n.3+96_3+97delinsAG
NR_111943.1:n.128_129delinsAG
NR_111944.1:n.119+96_119+97delinsAG
NM_001021.6:c.3+96_3+97delinsAG MANE Select	NP_001012.1:n.3+96_3+97delinsAG
NR_111944.2:n.139+96_139+97delinsAG
NR_111943.2:n.128_129delinsAG
NR_111944.3:n.32+96_32+97delinsAG