Canonical Allele Identifier: CA267568

Gene: RPS17

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82538982A>C , CM000677.2:g.82538982A>C	GRCh38
NC_000015.9:g.82823390A>C , CM000677.1:g.82823390A>C	GRCh37
NC_000015.8:g.80610445A>C	NCBI36
NG_009890.1:g.6256T>G
NG_009890.2:g.6563T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560229.6:n.481T>G
ENST00000562833.2:c.1506T>G	ENSP00000454786.2:p.Tyr502Ter
ENST00000642270.1:c.1513T>G	ENSP00000496443.1:n.1513T>G
ENST00000647841.1:c.159T>G MANE Select	ENSP00000498019.1:p.Tyr53Ter
ENST00000330244.10:c.159T>G	ENSP00000346046.5:p.Tyr53Ter
ENST00000558397.1:c.159T>G	ENSP00000452889.1:p.Tyr53Ter
ENST00000559776.1:n.443T>G
ENST00000560229.5:n.481T>G
ENST00000560612.1:n.166T>G
ENST00000560639.1:n.183T>G
ENST00000561068.5:c.231T>G
ENST00000561157.5:c.159T>G	ENSP00000453910.1:p.Tyr53Ter
ENST00000561440.1:n.1152T>G
NM_001021.4:c.159T>G	NP_001012.1:p.Tyr53Ter
NR_111943.1:n.481T>G
NR_111944.1:n.275T>G
NM_001021.6:c.159T>G MANE Select	NP_001012.1:p.Tyr53Ter
NR_111944.2:n.295T>G
NR_111943.2:n.481T>G
NR_111944.3:n.188T>G