Canonical Allele Identifier: CA371282987

Gene: RPS20

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.56073199A>C , CM000670.2:g.56073199A>C	GRCh38
NC_000008.10:g.56985758A>C , CM000670.1:g.56985758A>C	GRCh37
NC_000008.9:g.57148312A>C	NCBI36
NG_042872.1:g.6383T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001023.4:c.251T>G MANE Select	NP_001014.1:p.Ile84Ser
ENST00000009589.8:c.251T>G MANE Select	ENSP00000009589.3:p.Ile84Ser
NM_001023.3:c.251T>G	NP_001014.1:p.Ile84Ser
NM_001146227.1:c.251T>G	NP_001139699.1:p.Ile84Ser
NM_001146227.2:c.251T>G	NP_001139699.1:p.Ile84Ser
NM_001146227.3:c.251T>G	NP_001139699.1:p.Ile84Ser
ENST00000009589.7:c.251T>G	ENSP00000009589.3:p.Ile84Ser
ENST00000519606.5:c.*36T>G	ENSP00000429333.1:n.*36T>G
ENST00000519807.5:c.251T>G	ENSP00000429374.1:p.Ile84Ser
ENST00000520490.1:n.257T>G
ENST00000520627.1:c.86T>G	ENSP00000427860.1:p.Ile29Ser
ENST00000521262.5:c.251T>G	ENSP00000427788.1:p.Ile84Ser
ENST00000521289.5:n.665T>G
ENST00000523936.5:c.*487T>G	ENSP00000428104.1:n.*487T>G
ENST00000524349.5:c.86T>G	ENSP00000429049.1:p.Ile29Ser
ENST00000618656.1:c.251T>G	ENSP00000478703.1:p.Ile84Ser
ENST00000618656.2:c.233T>G	ENSP00000478703.2:p.Ile78Ser
ENST00000676461.1:c.251T>G	ENSP00000504670.1:p.Ile84Ser
ENST00000676918.1:c.251T>G	ENSP00000503327.1:p.Ile84Ser
ENST00000678039.1:c.251T>G	ENSP00000504154.1:p.Ile84Ser
ENST00000678683.1:c.251T>G	ENSP00000504123.1:p.Ile84Ser