Canonical Allele Identifier: CA716290696

Gene: RPS17

Linked Data

• dbSNP Id: rs1168049393
• gnomAD v3: 15-82540395-G-C
• gnomAD v4: 15-82540395-G-C
• MyVariant Identifiers: chr15:g.82824803G>C (hg19) ; chr15:g.82540395G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82540395G>C , CM000677.2:g.82540395G>C	GRCh38
NC_000015.9:g.82824803G>C , CM000677.1:g.82824803G>C	GRCh37
NC_000015.8:g.80611858G>C	NCBI36
NG_009890.1:g.4843C>G
NG_009890.2:g.5150C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560229.6:n.63C>G
ENST00000562833.2:c.1351-263C>G	ENSP00000454786.2:n.1351-263C>G
ENST00000642270.1:c.1358-263C>G	ENSP00000496443.1:n.1358-263C>G
ENST00000647841.1:c.3+31C>G MANE Select	ENSP00000498019.1:n.3+31C>G
ENST00000330244.10:c.3+31C>G	ENSP00000346046.5:n.3+31C>G
ENST00000558397.1:c.3+31C>G	ENSP00000452889.1:n.3+31C>G
ENST00000559273.1:n.31+31C>G
ENST00000559776.1:n.25C>G
ENST00000560229.5:n.63C>G
ENST00000560639.1:n.27+31C>G
ENST00000561157.5:c.3+31C>G	ENSP00000453910.1:n.3+31C>G
ENST00000562833.1:c.780-263C>G
NM_001021.4:c.3+31C>G	NP_001012.1:n.3+31C>G
NR_111943.1:n.63C>G
NR_111944.1:n.119+31C>G
NM_001021.6:c.3+31C>G MANE Select	NP_001012.1:n.3+31C>G
NR_111944.2:n.139+31C>G
NR_111943.2:n.63C>G
NR_111944.3:n.32+31C>G