Canonical Allele Identifier: CA2575814434

Gene: RPS17

Linked Data

• gnomAD v4: 15-82540436-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82540436G>A , CM000677.2:g.82540436G>A	GRCh38
NC_000015.9:g.82824844G>A , CM000677.1:g.82824844G>A	GRCh37
NC_000015.8:g.80611899G>A	NCBI36
NG_009890.1:g.4802C>T
NG_009890.2:g.5109C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560229.6:n.22C>T
ENST00000562833.2:c.1351-304C>T	ENSP00000454786.2:n.1351-304C>T
ENST00000642270.1:c.1358-304C>T	ENSP00000496443.1:n.1358-304C>T
ENST00000647841.1:c.-8C>T MANE Select	ENSP00000498019.1:n.-8C>T
ENST00000330244.10:c.-8C>T	ENSP00000346046.5:n.-8C>T
ENST00000558397.1:c.-8C>T	ENSP00000452889.1:n.-8C>T
ENST00000559273.1:n.21C>T
ENST00000560229.5:n.22C>T
ENST00000560639.1:n.17C>T
ENST00000561157.5:c.-8C>T	ENSP00000453910.1:n.-8C>T
ENST00000562833.1:c.780-304C>T
NM_001021.4:c.-8C>T	NP_001012.1:n.-8C>T
NR_111943.1:n.22C>T
NR_111944.1:n.109C>T
NM_001021.6:c.-8C>T MANE Select	NP_001012.1:n.-8C>T
NR_111944.2:n.129C>T
NR_111943.2:n.22C>T
NR_111944.3:n.22C>T