Canonical Allele Identifier: CA716290664

Gene: RPS17

Linked Data

• dbSNP Id: rs1205746416
• gnomAD v3: 15-82540343-G-T
• gnomAD v4: 15-82540343-G-T
• MyVariant Identifiers: chr15:g.82824751G>T (hg19) ; chr15:g.82540343G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82540343G>T , CM000677.2:g.82540343G>T	GRCh38
NC_000015.9:g.82824751G>T , CM000677.1:g.82824751G>T	GRCh37
NC_000015.8:g.80611806G>T	NCBI36
NG_009890.1:g.4895C>A
NG_009890.2:g.5202C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000560229.6:n.115C>A
ENST00000562833.2:c.1351-211C>A	ENSP00000454786.2:n.1351-211C>A
ENST00000642270.1:c.1358-211C>A	ENSP00000496443.1:n.1358-211C>A
ENST00000647841.1:c.3+83C>A MANE Select	ENSP00000498019.1:n.3+83C>A
ENST00000330244.10:c.3+83C>A	ENSP00000346046.5:n.3+83C>A
ENST00000558397.1:c.3+83C>A	ENSP00000452889.1:n.3+83C>A
ENST00000559273.1:n.31+83C>A
ENST00000559776.1:n.77C>A
ENST00000560229.5:n.115C>A
ENST00000560639.1:n.27+83C>A
ENST00000561157.5:c.3+83C>A	ENSP00000453910.1:n.3+83C>A
ENST00000562833.1:c.780-211C>A
NM_001021.4:c.3+83C>A	NP_001012.1:n.3+83C>A
NR_111943.1:n.115C>A
NR_111944.1:n.119+83C>A
NM_001021.6:c.3+83C>A MANE Select	NP_001012.1:n.3+83C>A
NR_111944.2:n.139+83C>A
NR_111943.2:n.115C>A
NR_111944.3:n.32+83C>A