Canonical Allele Identifier: CA2629987822

Gene: RPS17

Linked Data

• dbSNP Id: rs2150889055
• gnomAD v4: 15-82540369-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82540369G>A , CM000677.2:g.82540369G>A	GRCh38
NC_000015.9:g.82824777G>A , CM000677.1:g.82824777G>A	GRCh37
NC_000015.8:g.80611832G>A	NCBI36
NG_009890.1:g.4869C>T
NG_009890.2:g.5176C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560229.6:n.89C>T
ENST00000562833.2:c.1351-237C>T	ENSP00000454786.2:n.1351-237C>T
ENST00000642270.1:c.1358-237C>T	ENSP00000496443.1:n.1358-237C>T
ENST00000647841.1:c.3+57C>T MANE Select	ENSP00000498019.1:n.3+57C>T
ENST00000330244.10:c.3+57C>T	ENSP00000346046.5:n.3+57C>T
ENST00000558397.1:c.3+57C>T	ENSP00000452889.1:n.3+57C>T
ENST00000559273.1:n.31+57C>T
ENST00000559776.1:n.51C>T
ENST00000560229.5:n.89C>T
ENST00000560639.1:n.27+57C>T
ENST00000561157.5:c.3+57C>T	ENSP00000453910.1:n.3+57C>T
ENST00000562833.1:c.780-237C>T
NM_001021.4:c.3+57C>T	NP_001012.1:n.3+57C>T
NR_111943.1:n.89C>T
NR_111944.1:n.119+57C>T
NM_001021.6:c.3+57C>T MANE Select	NP_001012.1:n.3+57C>T
NR_111944.2:n.139+57C>T
NR_111943.2:n.89C>T
NR_111944.3:n.32+57C>T