Canonical Allele Identifier: CA2191414130

Gene: RPS17

Linked Data

• dbSNP Id: rs2034328359
• gnomAD v4: 15-82540340-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82540340A>G , CM000677.2:g.82540340A>G	GRCh38
NC_000015.9:g.82824748A>G , CM000677.1:g.82824748A>G	GRCh37
NC_000015.8:g.80611803A>G	NCBI36
NG_009890.1:g.4898T>C
NG_009890.2:g.5205T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000560229.6:n.118T>C
ENST00000562833.2:c.1351-208T>C	ENSP00000454786.2:n.1351-208T>C
ENST00000642270.1:c.1358-208T>C	ENSP00000496443.1:n.1358-208T>C
ENST00000647841.1:c.3+86T>C MANE Select	ENSP00000498019.1:n.3+86T>C
ENST00000330244.10:c.3+86T>C	ENSP00000346046.5:n.3+86T>C
ENST00000558397.1:c.3+86T>C	ENSP00000452889.1:n.3+86T>C
ENST00000559273.1:n.31+86T>C
ENST00000559776.1:n.80T>C
ENST00000560229.5:n.118T>C
ENST00000560639.1:n.27+86T>C
ENST00000561157.5:c.3+86T>C	ENSP00000453910.1:n.3+86T>C
ENST00000562833.1:c.780-208T>C
NM_001021.4:c.3+86T>C	NP_001012.1:n.3+86T>C
NR_111943.1:n.118T>C
NR_111944.1:n.119+86T>C
NM_001021.6:c.3+86T>C MANE Select	NP_001012.1:n.3+86T>C
NR_111944.2:n.139+86T>C
NR_111943.2:n.118T>C
NR_111944.3:n.32+86T>C