Canonical Allele Identifier: CA10588481

Gene: RPS24

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78033902A>G , CM000672.2:g.78033902A>G	GRCh38
NC_000010.10:g.79793660A>G , CM000672.1:g.79793660A>G	GRCh37
NC_000010.9:g.79463666A>G	NCBI36
NG_012633.1:g.5143A>G
NG_029648.1:g.639T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360830.9:c.1A>G	ENSP00000354074.5:p.Met1Val
ENST00000372360.9:c.1A>G MANE Select	ENSP00000361435.4:p.Met1Val
ENST00000440692.6:c.1A>G	ENSP00000414321.1:p.Met1Val
ENST00000464716.6:c.1A>G	ENSP00000494231.1:p.Met1Val
ENST00000465692.2:n.12A>G
ENST00000466129.6:n.17A>G
ENST00000476545.6:c.1A>G	ENSP00000494169.1:p.Met1Val
ENST00000478655.6:n.40A>G
ENST00000485708.7:n.40A>G
ENST00000613865.5:c.1A>G	ENSP00000478869.2:p.Met1Val
ENST00000645440.1:c.1A>G	ENSP00000496738.1:p.Met1Val
ENST00000645698.1:n.29A>G
ENST00000360830.8:c.1A>G	ENSP00000354074.4:p.Met1Val
ENST00000372360.7:c.1A>G	ENSP00000361435.3:p.Met1Val
ENST00000435275.5:c.1A>G	ENSP00000415549.1:p.Met1Val
ENST00000440692.5:c.1A>G	ENSP00000414321.1:p.Met1Val
ENST00000464716.5:n.29A>G
ENST00000466129.5:n.17A>G
ENST00000476545.5:n.25A>G
ENST00000478655.5:n.40A>G
ENST00000485708.6:n.59A>G
ENST00000613865.4:c.1A>G	ENSP00000478869.1:p.Met1Val
NM_001026.4:c.1A>G	NP_001017.1:p.Met1Val
NM_001142282.1:c.1A>G	NP_001135754.1:p.Met1Val
NM_001142283.1:c.1A>G	NP_001135755.1:p.Met1Val
NM_001142284.1:c.1A>G	NP_001135756.1:p.Met1Val
NM_001142285.1:c.1A>G	NP_001135757.1:p.Met1Val
NM_033022.3:c.1A>G	NP_148982.1:p.Met1Val
NM_001142285.2:c.1A>G	NP_001135757.1:p.Met1Val
NM_033022.4:c.1A>G MANE Select	NP_148982.1:p.Met1Val
NM_001026.5:c.1A>G	NP_001017.1:p.Met1Val
NM_001142282.2:c.1A>G	NP_001135754.1:p.Met1Val
NM_001142283.2:c.1A>G	NP_001135755.1:p.Met1Val
NM_001142284.2:c.1A>G	NP_001135756.1:p.Met1Val