Canonical Allele Identifier: CA2629987752

Gene: RPS17

Linked Data

• gnomAD v4: 15-82540337-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82540337C>A , CM000677.2:g.82540337C>A	GRCh38
NC_000015.9:g.82824745C>A , CM000677.1:g.82824745C>A	GRCh37
NC_000015.8:g.80611800C>A	NCBI36
NG_009890.1:g.4901G>T
NG_009890.2:g.5208G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000560229.6:n.121G>T
ENST00000562833.2:c.1351-205G>T	ENSP00000454786.2:n.1351-205G>T
ENST00000642270.1:c.1358-205G>T	ENSP00000496443.1:n.1358-205G>T
ENST00000647841.1:c.3+89G>T MANE Select	ENSP00000498019.1:n.3+89G>T
ENST00000330244.10:c.3+89G>T	ENSP00000346046.5:n.3+89G>T
ENST00000558397.1:c.3+89G>T	ENSP00000452889.1:n.3+89G>T
ENST00000559273.1:n.31+89G>T
ENST00000559776.1:n.83G>T
ENST00000560229.5:n.121G>T
ENST00000560639.1:n.27+89G>T
ENST00000561157.5:c.3+89G>T	ENSP00000453910.1:n.3+89G>T
ENST00000562833.1:c.780-205G>T
NM_001021.4:c.3+89G>T	NP_001012.1:n.3+89G>T
NR_111943.1:n.121G>T
NR_111944.1:n.119+89G>T
NM_001021.6:c.3+89G>T MANE Select	NP_001012.1:n.3+89G>T
NR_111944.2:n.139+89G>T
NR_111943.2:n.121G>T
NR_111944.3:n.32+89G>T