Canonical Allele Identifier: CA619052080

Gene: RPS17

Linked Data

• dbSNP Id: rs751731453
• gnomAD v2: 15-82824860-G-C
• gnomAD v4: 15-82540452-G-C
• MyVariant Identifiers: chr15:g.82824860G>C (hg19) ; chr15:g.82540452G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82540452G>C , CM000677.2:g.82540452G>C	GRCh38
NC_000015.9:g.82824860G>C , CM000677.1:g.82824860G>C	GRCh37
NC_000015.8:g.80611915G>C	NCBI36
NG_009890.1:g.4786C>G
NG_009890.2:g.5093C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560229.6:n.6C>G
ENST00000562833.2:c.1351-320C>G	ENSP00000454786.2:n.1351-320C>G
ENST00000642270.1:c.1358-320C>G	ENSP00000496443.1:n.1358-320C>G
ENST00000647841.1:c.-24C>G MANE Select	ENSP00000498019.1:n.-24C>G
ENST00000330244.10:c.-24C>G	ENSP00000346046.5:n.-24C>G
ENST00000559273.1:n.5C>G
ENST00000560229.5:n.6C>G
ENST00000560639.1:n.1C>G
ENST00000561157.5:c.-24C>G	ENSP00000453910.1:n.-24C>G
ENST00000562833.1:c.780-320C>G
NM_001021.4:c.-24C>G	NP_001012.1:n.-24C>G
NR_111943.1:n.6C>G
NR_111944.1:n.93C>G
NM_001021.6:c.-24C>G MANE Select	NP_001012.1:n.-24C>G
NR_111944.2:n.113C>G
NR_111943.2:n.6C>G
NR_111944.3:n.6C>G