Canonical Allele Identifier: CA393409044

Gene: RPS17

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82538986C>T , CM000677.2:g.82538986C>T	GRCh38
NC_000015.9:g.82823394C>T , CM000677.1:g.82823394C>T	GRCh37
NC_000015.8:g.80610449C>T	NCBI36
NG_009890.1:g.6252G>A
NG_009890.2:g.6559G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560229.6:n.478-1G>A
ENST00000562833.2:c.1503-1G>A	ENSP00000454786.2:n.1503-1G>A
ENST00000642270.1:c.1510-1G>A	ENSP00000496443.1:n.1510-1G>A
ENST00000647841.1:c.156-1G>A MANE Select	ENSP00000498019.1:n.156-1G>A
ENST00000330244.10:c.156-1G>A	ENSP00000346046.5:n.156-1G>A
ENST00000558397.1:c.156-1G>A	ENSP00000452889.1:n.156-1G>A
ENST00000559776.1:n.440-1G>A
ENST00000560229.5:n.478-1G>A
ENST00000560612.1:n.163-1G>A
ENST00000560639.1:n.180-1G>A
ENST00000561068.5:c.228-1G>A
ENST00000561157.5:c.156-1G>A	ENSP00000453910.1:n.156-1G>A
ENST00000561440.1:n.1148G>A
NM_001021.4:c.156-1G>A	NP_001012.1:n.156-1G>A
NR_111943.1:n.478-1G>A
NR_111944.1:n.272-1G>A
NM_001021.6:c.156-1G>A MANE Select	NP_001012.1:n.156-1G>A
NR_111944.2:n.292-1G>A
NR_111943.2:n.478-1G>A
NR_111944.3:n.185-1G>A