Canonical Allele Identifier: CA2575814428

Gene: RPS17

Linked Data

• gnomAD v4: 15-82540396-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82540396A>G , CM000677.2:g.82540396A>G	GRCh38
NC_000015.9:g.82824804A>G , CM000677.1:g.82824804A>G	GRCh37
NC_000015.8:g.80611859A>G	NCBI36
NG_009890.1:g.4842T>C
NG_009890.2:g.5149T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560229.6:n.62T>C
ENST00000562833.2:c.1351-264T>C	ENSP00000454786.2:n.1351-264T>C
ENST00000642270.1:c.1358-264T>C	ENSP00000496443.1:n.1358-264T>C
ENST00000647841.1:c.3+30T>C MANE Select	ENSP00000498019.1:n.3+30T>C
ENST00000330244.10:c.3+30T>C	ENSP00000346046.5:n.3+30T>C
ENST00000558397.1:c.3+30T>C	ENSP00000452889.1:n.3+30T>C
ENST00000559273.1:n.31+30T>C
ENST00000559776.1:n.24T>C
ENST00000560229.5:n.62T>C
ENST00000560639.1:n.27+30T>C
ENST00000561157.5:c.3+30T>C	ENSP00000453910.1:n.3+30T>C
ENST00000562833.1:c.780-264T>C
NM_001021.4:c.3+30T>C	NP_001012.1:n.3+30T>C
NR_111943.1:n.62T>C
NR_111944.1:n.119+30T>C
NM_001021.6:c.3+30T>C MANE Select	NP_001012.1:n.3+30T>C
NR_111944.2:n.139+30T>C
NR_111943.2:n.62T>C
NR_111944.3:n.32+30T>C