Canonical Allele Identifier: CA526386741

Gene: RPS27

Linked Data

• dbSNP Id: rs1174236551
• gnomAD v2: 1-153963318-T-G
• gnomAD v4: 1-153990842-T-G
• MyVariant Identifiers: chr1:g.153963318T>G (hg19) ; chr1:g.153990842T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153990842T>G , CM000663.2:g.153990842T>G	GRCh38
NC_000001.10:g.153963318T>G , CM000663.1:g.153963318T>G	GRCh37
NC_000001.9:g.152229942T>G	NCBI36
NG_053102.2:g.5088T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643794.1:c.6+40T>G	ENSP00000495765.1:n.6+40T>G
ENST00000651669.1:c.6+40T>G MANE Select	ENSP00000499044.1:n.6+40T>G
ENST00000368567.4:c.6+40T>G	ENSP00000357555.4:n.6+40T>G
ENST00000392558.4:c.6+40T>G	ENSP00000376341.4:n.6+40T>G
ENST00000477151.1:n.40+40T>G
ENST00000493224.5:n.80T>G
NM_001030.4:c.6+40T>G	NP_001021.1:n.6+40T>G
NM_001030.6:c.6+40T>G MANE Select	NP_001021.1:n.6+40T>G
NM_001349946.1:c.-212+40T>G	NP_001336875.1:n.-212+40T>G
NM_001349947.1:c.-283T>G	NP_001336876.1:n.-283T>G
NM_001349946.2:c.-212+40T>G	NP_001336875.1:n.-212+40T>G
NM_001349947.2:c.-283T>G	NP_001336876.1:n.-283T>G