Canonical Allele Identifier: CA619052075

Gene: RPS17

Linked Data

• dbSNP Id: rs1161696842
• gnomAD v2: 15-82824831-T-C
• gnomAD v4: 15-82540423-T-C
• MyVariant Identifiers: chr15:g.82824831T>C (hg19) ; chr15:g.82540423T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82540423T>C , CM000677.2:g.82540423T>C	GRCh38
NC_000015.9:g.82824831T>C , CM000677.1:g.82824831T>C	GRCh37
NC_000015.8:g.80611886T>C	NCBI36
NG_009890.1:g.4815A>G
NG_009890.2:g.5122A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560229.6:n.35A>G
ENST00000562833.2:c.1351-291A>G	ENSP00000454786.2:n.1351-291A>G
ENST00000642270.1:c.1358-291A>G	ENSP00000496443.1:n.1358-291A>G
ENST00000647841.1:c.3+3A>G MANE Select	ENSP00000498019.1:n.3+3A>G
ENST00000330244.10:c.3+3A>G	ENSP00000346046.5:n.3+3A>G
ENST00000558397.1:c.3+3A>G	ENSP00000452889.1:n.3+3A>G
ENST00000559273.1:n.31+3A>G
ENST00000560229.5:n.35A>G
ENST00000560639.1:n.27+3A>G
ENST00000561157.5:c.3+3A>G	ENSP00000453910.1:n.3+3A>G
ENST00000562833.1:c.780-291A>G
NM_001021.4:c.3+3A>G	NP_001012.1:n.3+3A>G
NR_111943.1:n.35A>G
NR_111944.1:n.119+3A>G
NM_001021.6:c.3+3A>G MANE Select	NP_001012.1:n.3+3A>G
NR_111944.2:n.139+3A>G
NR_111943.2:n.35A>G
NR_111944.3:n.32+3A>G