Canonical Allele Identifier: CA2629987782

Gene: RPS17

Linked Data

• gnomAD v4: 15-82540361-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82540361G>T , CM000677.2:g.82540361G>T	GRCh38
NC_000015.9:g.82824769G>T , CM000677.1:g.82824769G>T	GRCh37
NC_000015.8:g.80611824G>T	NCBI36
NG_009890.1:g.4877C>A
NG_009890.2:g.5184C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560229.6:n.97C>A
ENST00000562833.2:c.1351-229C>A	ENSP00000454786.2:n.1351-229C>A
ENST00000642270.1:c.1358-229C>A	ENSP00000496443.1:n.1358-229C>A
ENST00000647841.1:c.3+65C>A MANE Select	ENSP00000498019.1:n.3+65C>A
ENST00000330244.10:c.3+65C>A	ENSP00000346046.5:n.3+65C>A
ENST00000558397.1:c.3+65C>A	ENSP00000452889.1:n.3+65C>A
ENST00000559273.1:n.31+65C>A
ENST00000559776.1:n.59C>A
ENST00000560229.5:n.97C>A
ENST00000560639.1:n.27+65C>A
ENST00000561157.5:c.3+65C>A	ENSP00000453910.1:n.3+65C>A
ENST00000562833.1:c.780-229C>A
NM_001021.4:c.3+65C>A	NP_001012.1:n.3+65C>A
NR_111943.1:n.97C>A
NR_111944.1:n.119+65C>A
NM_001021.6:c.3+65C>A MANE Select	NP_001012.1:n.3+65C>A
NR_111944.2:n.139+65C>A
NR_111943.2:n.97C>A
NR_111944.3:n.32+65C>A