Canonical Allele Identifier: CA972064502

Gene: RPS17

Linked Data

• dbSNP Id: rs1245251898
• gnomAD v3: 15-82540453-G-T
• gnomAD v4: 15-82540453-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82540453G>T , CM000677.2:g.82540453G>T	GRCh38
NC_000015.9:g.82824861G>T , CM000677.1:g.82824861G>T	GRCh37
NC_000015.8:g.80611916G>T	NCBI36
NG_009890.1:g.4785C>A
NG_009890.2:g.5092C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560229.6:n.5C>A
ENST00000562833.2:c.1351-321C>A	ENSP00000454786.2:n.1351-321C>A
ENST00000642270.1:c.1358-321C>A	ENSP00000496443.1:n.1358-321C>A
ENST00000647841.1:c.-25C>A MANE Select	ENSP00000498019.1:n.-25C>A
ENST00000330244.10:c.-25C>A	ENSP00000346046.5:n.-25C>A
ENST00000559273.1:n.4C>A
ENST00000560229.5:n.5C>A
ENST00000561157.5:c.-25C>A	ENSP00000453910.1:n.-25C>A
ENST00000562833.1:c.780-321C>A
NM_001021.4:c.-25C>A	NP_001012.1:n.-25C>A
NR_111943.1:n.5C>A
NR_111944.1:n.92C>A
NM_001021.6:c.-25C>A MANE Select	NP_001012.1:n.-25C>A
NR_111944.2:n.112C>A
NR_111943.2:n.5C>A
NR_111944.3:n.5C>A