Canonical Allele Identifier: CA716290652

Gene: RPS17

Linked Data

• dbSNP Id: rs1209736478
• gnomAD v3: 15-82540329-CT-C
• gnomAD v4: 15-82540329-CT-C
• MyVariant Identifiers: chr15:g.82824738del (hg19) ; chr15:g.82540330del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82540331del , CM000677.2:g.82540331del	GRCh38
NC_000015.9:g.82824739del , CM000677.1:g.82824739del	GRCh37
NC_000015.8:g.80611794del	NCBI36
NG_009890.1:g.4908del
NG_009890.2:g.5215del

Transcript Alleles

HGVS	Amino-acid change
ENST00000560229.6:n.128del
ENST00000562833.2:c.1351-198del	ENSP00000454786.2:n.1351-198del
ENST00000642270.1:c.1358-198del	ENSP00000496443.1:n.1358-198del
ENST00000647841.1:c.3+96del MANE Select	ENSP00000498019.1:n.3+96del
ENST00000330244.10:c.3+96del	ENSP00000346046.5:n.3+96del
ENST00000558397.1:c.3+96del	ENSP00000452889.1:n.3+96del
ENST00000559273.1:n.31+96del
ENST00000559776.1:n.90del
ENST00000560229.5:n.128del
ENST00000560639.1:n.27+96del
ENST00000561157.5:c.3+96del	ENSP00000453910.1:n.3+96del
ENST00000562833.1:c.780-198del
NM_001021.4:c.3+96del	NP_001012.1:n.3+96del
NR_111943.1:n.128del
NR_111944.1:n.119+96del
NM_001021.6:c.3+96del MANE Select	NP_001012.1:n.3+96del
NR_111944.2:n.139+96del
NR_111943.2:n.128del
NR_111944.3:n.32+96del