Canonical Allele Identifier: CA658820698

Gene: RPS29

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.49586055A>C , CM000676.2:g.49586055A>C	GRCh38
NC_000014.8:g.50052773A>C , CM000676.1:g.50052773A>C	GRCh37
NC_000014.7:g.49122523A>C	NCBI36
NG_050638.2:g.17656T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245458.11:c.63-6T>G MANE Select	ENSP00000245458.7:n.63-6T>G
ENST00000554075.2:c.63-6T>G	ENSP00000496485.1:n.63-6T>G
ENST00000556230.2:c.63-6T>G	ENSP00000495033.1:n.63-6T>G
ENST00000245458.10:c.63-6T>G	ENSP00000245458.6:n.63-6T>G
ENST00000396020.7:c.63-6T>G	ENSP00000379339.3:n.63-6T>G
ENST00000554075.1:n.75-6T>G
ENST00000556230.1:n.93-6T>G
ENST00000557111.5:c.54-6T>G	ENSP00000478117.1:n.54-6T>G
ENST00000557367.2:n.297T>G
ENST00000557519.1:n.42-6T>G
ENST00000611563.1:c.63-6T>G	ENSP00000479892.1:n.63-6T>G
NM_001030001.2:c.63-6T>G	NP_001025172.1:n.63-6T>G
NM_001032.4:c.63-6T>G	NP_001023.1:n.63-6T>G
NM_001030001.3:c.63-6T>G	NP_001025172.1:n.63-6T>G
NM_001351375.1:c.54-6T>G	NP_001338304.1:n.54-6T>G
NM_001030001.4:c.63-6T>G	NP_001025172.1:n.63-6T>G
NM_001032.5:c.63-6T>G MANE Select	NP_001023.1:n.63-6T>G
NM_001351375.2:c.54-6T>G	NP_001338304.1:n.54-6T>G